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all-genes.txt
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all-genes.txt
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989
990
991
992
993
994
995
996
997
998
999
1000
ENSG00000261657
SLC25A26
INTRA-MITOCHONDRIAL METHYLATION DEFICIENCY
20661
115286
ENSG00000252952
RNU6-58P
42548
100873766
ENSG00000229558
SACS-AS1
39835
100506680
ENSG00000232977
LINC00327
42009
100506697
ENSG00000236520
GPC6-AS1
39909
100873972
ENSG00000227640
SOX21-AS1
39807
100507533
ENSG00000223392
CLDN10-AS1
39907
100874194
ENSG00000228741
RP11-309I15.1
221178
ENSG00000247400
DNAJC3-AS1
39808
100289274
ENSG00000252695
MIR2276
37313
100313842
ENSG00000227213
SPATA13-AS1
39905
100874231
ENSG00000243300
LINC00359
42679
100887754
ENSG00000263399
MIR3170
38282
100422881
ENSG00000229918
DOCK9-AS1
40672
100874096
ENSG00000261530
BTC
1121
685
ENSG00000207298
RNU6-83P
42573
100873782
ENSG00000199767
RNU6-78P
42568
100873778
ENSG00000260992
DOCK9-AS2
43696
100861541
ENSG00000260334
GAST
4164
2520
ENSG00000228889
UBAC2-AS1
42502
100289373
ENSG00000207719
MIR623
32879
693208
ENSG00000263615
MIR4306
38350
100422861
ENSG00000227659
CLYBL-AS2
39894
100874063
ENSG00000234303
CLYBL-AS1
39893
101927465
ENSG00000230641
USP12-AS2
39962
100874071
ENSG00000207500
SNORD102
10099
26771
ENSG00000260738
LINC00554
43697
100861542
ENSG00000207051
SNORA27
32617
619499
ENSG00000252499
RNU6-63P
42553
100873768
ENSG00000261125
HAP1
4812
9001
ENSG00000234650
PCCA-AS1
39901
100885777
ENSG00000247381
PDX1-AS1
43698
100861550
ENSG00000261485
PAN3-AS1
39932
100288730
ENSG00000200840
RNU6-82P
42572
100873781
ENSG00000233009
NALCN-AS1
42743
100885778
ENSG00000202237
RNU6-53P
42543
100873762
ENSG00000265164
MIR2681
41532
100616110
ENSG00000179141
MTUS2-AS1
40924
100874107
ENSG00000264482
MIR4705
41567
100616239
ENSG00000224329
LINC00297
39210
100874059
ENSG00000243319
FGF14-IT1
42774
283480
ENSG00000224405
LINC00572
43722
100861573
ENSG00000234445
FGF14-AS1
40237
100874081
ENSG00000122043
LINC00544
43679
440131
ENSG00000272143
FGF14-AS2
44368
283481
ENSG00000232117
LINC00384
42711
101928980
ENSG00000252928
RNU6-64P
42554
100873769
ENSG00000250878
METTL21EP
41948
121952
ENSG00000236463
LINC00427
42762
100507040
ENSG00000234551
RP11-123H22.1
101930454
ENSG00000232307
DAOA-AS1
30243
282706
ENSG00000238121
LINC00426
42761
100188949
ENSG00000226620
LINC00343
42500
144920
ENSG00000261577
JUP
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA FAMILIAL 12
6207
3728
ENSG00000261577
JUP
NAXOS DISEASE
6207
3728
ENSG00000233532
LINC00460
42809
728192
ENSG00000272274
LINC00551
43691
283483
ENSG00000230156
LINC00443
42780
100874173
ENSG00000237879
LINC00398
42727
100874158
ENSG00000224743
TEX26-AS1
42784
100507064
ENSG00000221650
MIR1267
35335
100302286
ENSG00000227248
FAM155A-IT1
41503
100874375
ENSG00000236094
LINC00545
43680
440132
ENSG00000236242
MYO16-AS1
39913
100885782
ENSG00000261163
LEPREL4
10609
ENSG00000265841
MIR548X
38248
100422920
ENSG00000234854
LINC00676
44394
101409253
ENSG00000224821
COL4A2-AS2
39849
100129836
ENSG00000237637
FRY-AS1
39725
100507099
ENSG00000232814
COL4A2-AS1
40156
100874203
ENSG00000225870
LINC00368
42690
101927802
ENSG00000226968
LINC00423
42758
100874167
ENSG00000261258
FKBP10
Bruck syndrome 1
18169
60681
ENSG00000261258
FKBP10
OSTEOGENESIS IMPERFECTA TYPE XI
18169
60681
ENSG00000226903
LINC00354
42672
101928616
ENSG00000224924
LINC00320
19690
387486
ENSG00000224243
LINC00403
42733
100505996
ENSG00000260102
LINC01070
49110
101928698
ENSG00000260343
LINC01043
49031
101928752
ENSG00000232684
ATP11A-AS1
40645
100874205
ENSG00000238265
LINC00317
23126
378828
ENSG00000236581
STARD13-AS
40873
100874241
ENSG00000233997
AP000475.2
101927821
ENSG00000225083
GRTP1-AS1
39917
101930262
ENSG00000225083
GRTP1-AS1
39917
101930007
ENSG00000233215
AP000472.2
101927843
ENSG00000227208
LINC00552
43692
100130386
ENSG00000272695
GAS6-AS2
43694
100506394
ENSG00000184856
LINC00308
16023
54143
ENSG00000260753
NT5C3B
28300
115024
ENSG00000212051
MIR320C2
35387
100302195
ENSG00000226921
LINC00454
42802
100874178
ENSG00000229373
LINC00452
42800
643365
ENSG00000215405
GOLGA6L6
37225
727832
ENSG00000225179
LINC00457
42805
100874179
ENSG00000260910
LINC00565
43709
100861555
ENSG00000264539
MIR548AR
43455
100847035
ENSG00000265450
MIR4502
41534
100616227
ENSG00000236036
LINC00445
42782
100507114
ENSG00000207203
RNU6-71P
42561
100873774
ENSG00000261631
KLHL10
SPERMATOGENIC FAILURE 11
18829
317719
ENSG00000230031
POTEB2
48327
100996331
ENSG00000230031
POTEB2
48327
100287399
ENSG00000259896
KLHL11
19008
55175
ENSG00000223685
LINC00571
43721
100874188
ENSG00000236354
LINC00437
42772
101929121
ENSG00000228592
AP000459.4
266917
ENSG00000252795
RNU6-56P
42546
100873764
ENSG00000264171
MIR4305
38301
100422940
ENSG00000138593
SECISBP2L
28997
9728
ENSG00000230710
LINC00332
42049
100874127
ENSG00000215483
LINC00598
42770
646982
ENSG00000211491
MIR320D1
35386
100313896
ENSG00000207652
MIR621
32877
693206
ENSG00000168852
TPTE2P5
42356
100616668
ENSG00000233917
POTEB
33734
100996331
ENSG00000233917
POTEB
33734
100288966
ENSG00000233917
POTEB
33734
100287399
ENSG00000233917
POTEB
33734
317754
ENSG00000166157
TPTE
12023
7179
ENSG00000260245
ACLY
115
47
ENSG00000239827
SUGT1P3
20513
283507
ENSG00000264226
MIR3168
38249
100422878
ENSG00000223280
RNU6-57P
42547
100873765
ENSG00000224832
AP000469.2
101927869
ENSG00000205240
OR7E36P
8409
100506759
ENSG00000265485
RP11-449D8.1
729950
ENSG00000264190
MIR5006
43495
100847026
ENSG00000260703
TTC25
Primary Ciliary Dyskinesia with Left-Right Body Asymmetry Randomization
25280
83538
ENSG00000166351
POTED
23822
388468
ENSG00000166351
POTED
23822
339010
ENSG00000166351
POTED
23822
317754
ENSG00000233725
LINC00284
26981
121838
ENSG00000260283
CNP
2158
1267
ENSG00000260372
AQP4-AS1
26399
147429
ENSG00000168675
LDLRAD4
1224
753
ENSG00000227258
SMIM2-AS1
42674
101929212
ENSG00000265369
U3
728606
ENSG00000235285
SMIM2-IT1
41492
100874377
ENSG00000237361
LINC01071
49111
400128
ENSG00000262684
DNAJC7
12392
7266
ENSG00000188992
LIPI
HYPERTRIGLYCERIDEMIA FAMILIAL
18821
149998
ENSG00000235097
LINC00330
42047
144817
ENSG00000252055
RNU6-69P
42559
100873773
ENSG00000199477
SNORA31
32621
677814
ENSG00000185272
RBM11
9897
54033
ENSG00000182974
OR4M2
15373
390538
ENSG00000226983
AP000235.2
339622
ENSG00000260770
NKIRAS2
17898
28511
ENSG00000183706
OR4N4
15375
283694
ENSG00000170919
TPT1-AS1
43686
100190939
ENSG00000259261
IGHV4OR15-8
5658
642131
ENSG00000155304
HSPA13
11375
6782
ENSG00000260320
ZNF385C
33722
201181
ENSG00000197414
GOLGA6L1
37444
645202
ENSG00000197414
GOLGA6L1
37444
440243
ENSG00000197414
GOLGA6L1
37444
283767
ENSG00000260178
DHX58
29517
79132
ENSG00000235903
CPB2-AS1
39898
100509894
ENSG00000261097
LINC00563
43707
100861554
ENSG00000252385
RNU6-68P
42558
100873772
ENSG00000166200
COPS2
30747
9318
ENSG00000155307
SAMSN1
10528
64092
ENSG00000259958
KAT2A
4201
2648
ENSG00000243440
AF165138.7
388813
ENSG00000260325
HSPB9
30589
94086
ENSG00000224517
HTR2A-AS1
40289
100874082
ENSG00000261378
RAB5C
9785
5878
ENSG00000153575
TUBGCP5
18600
114791
ENSG00000227848
SUCLA2-AS1
39965
101929410
ENSG00000229111
MED4-AS1
39213
100873965
ENSG00000231473
LINC00441
42778
100862704
ENSG00000180530
NRIP1
8001
8204
ENSG00000233610
LINC00462
42811
100129597
ENSG00000137824
RMDN3
25550
55177
ENSG00000261371
PECAM1
8823
5175
ENSG00000181358
CTAGE10P
37288
220429
ENSG00000264864
MIR3613
38964
100500908
ENSG00000231607
DLEU2
13748
406948
ENSG00000265888
RP11-408H20.2
101927698
ENSG00000185433
LINC00158
1283
54072
ENSG00000266729
RP11-534N16.1
101927718
ENSG00000208006
MIR16-1
31545
406950
ENSG00000234883
MIR155HG
35460
406947
ENSG00000234883
MIR155HG
35460
114614
ENSG00000232150
ST13P4
18487
145165
ENSG00000260583
LINC00515
16019
282566
ENSG00000263304
MILR1
27570
284021
ENSG00000137880
GCHFR
4194
2644
ENSG00000237152
DLEU7-AS1
39966
100874074
ENSG00000233672
RNASEH2B-AS1
39967
100874255
ENSG00000262917
POLG2
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONSAUTOSOMAL RECESSIVE 2
9180
11232
ENSG00000260389
WBP11P1
26250
441818
ENSG00000104129
DNAJC17
25556
55192
ENSG00000177150
FAM210A
28346
125228
ENSG00000123201
GUCY1B2
4686
2974
ENSG00000155313
USP25
12624
29761
ENSG00000197934
AP001597.1
100996571
ENSG00000266133
MIR4759
41575
100616243
ENSG00000226792
LINC00371
42693
647166