chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
12
39062271
39062272
T
G
1
GENIC
homozygous
50196927
12
39062276
39062277
C
A
1
GENIC
homozygous
50196929
12
39062278
39062279
T
G
1
GENIC
homozygous
50196931
12
39062313
39062314
C
G
1
GENIC
homozygous
50196939
12
39062316
39062317
C
G
1
GENIC
homozygous
50196941
12
39063853
39063854
A
G
21
GENIC
possibly homozygous
50196949
12
39063937
39063938
A
-
2
GENIC
heterozygous
50196951
12
39064368
39064369
A
AAAAAATGTGGCTGCACACATGCTCAGGCTGCTGAGAC
2
GENIC
homozygous
50511147
12
39064446
39064447
A
ACTCAGG
7
GENIC
homozygous
50196955
12
39064457
39064458
G
GTAGTTAGGAATTCC
3
GENIC
heterozygous
50196957
12
39064543
39064544
A
C
1
GENIC
homozygous
50196960
12
39065851
39065852
A
G
26
GENIC
possibly homozygous
50196962
12
39066303
39066304
A
T
11
GENIC
homozygous
50451499
12
39066321
39066322
A
G
13
GENIC
homozygous
50196964
12
39067604
39067605
A
G
11
GENIC
homozygous
50196966
12
39067610
39067611
T
G
15
GENIC
homozygous
50196968
12
39067988
39067989
C
CT
24
GENIC
possibly homozygous
50196970
12
39068348
39068349
T
C
11
GENIC
homozygous
50196972
12
39068522
39068523
C
CAAAAAAAAAA
1
GENIC
homozygous
50542484
12
39068946
39068947
A
T
16
GENIC
possibly homozygous
50591959
12
39069244
39069245
T
A
7
GENIC
heterozygous
50468869
12
39069414
39069415
T
C
18
GENIC
possibly homozygous
50196976
12
39069562
39069563
G
A
15
GENIC
homozygous
50196978
12
39069704
39069705
T
C
26
GENIC
possibly homozygous
50196980
12
39069828
39069829
A
C
20
GENIC
homozygous
50196982
12
39070567
39070568
T
C
31
GENIC
homozygous
50196986
12
39070597
39070598
C
G
27
GENIC
possibly homozygous
50196988
12
39071512
39071513
A
G
10
GENIC
homozygous
50196990
12
39071785
39071786
T
C
11
GENIC
homozygous
50196992
12
39072705
39072707
AA
--
1
GENIC
homozygous
50542488
12
39072707
39072708
A
G
1
GENIC
homozygous
50571183
12
39074836
39074837
C
T
27
GENIC
homozygous
50591960
12
39075203
39075204
T
C
24
GENIC
possibly homozygous
50196998
12
39075406
39075407
A
G
24
GENIC
possibly homozygous
50197000
12
39076460
39076461
A
G
35
GENIC
possibly homozygous
50197004
12
39077119
39077120
C
T
21
GENIC
homozygous
50591961
12
39077747
39077748
T
A
28
GENIC
possibly homozygous
50197006
12
39078019
39078020
C
T
25
GENIC
homozygous
50197008
12
39078347
39078348
T
C
11
GENIC
homozygous
50451502
12
39078913
39078914
G
GTCTGTCTCTC
2
GENIC
homozygous
50558882
12
39079435
39079436
C
T
22
GENIC
heterozygous
50197012
12
39080014
39080015
G
C
14
GENIC
homozygous
50197014
12
39080071
39080072
T
C
14
GENIC
homozygous
50451503
12
39080519
39080520
T
G
23
GENIC
possibly homozygous
50197016
12
39080596
39080597
G
T
21
GENIC
possibly homozygous
50197018
12
39080755
39080756
G
T
14
GENIC
possibly homozygous
50197020
12
39080982
39080983
G
A
4
GENIC
homozygous
50197024
12
39080989
39080990
A
T
4
GENIC
heterozygous
50451505
12
39081000
39081001
T
C
7
GENIC
heterozygous
50197026
12
39081561
39081562
A
C
26
GENIC
homozygous
50197028
12
39082665
39082666
T
C
1
GENIC
homozygous
50197034
12
39083082
39083083
G
T
13
GENIC
heterozygous
50451507
12
39084777
39084778
C
CT
4
GENIC
heterozygous
50591962
