chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
12
34993599
34993600
G
A
8
GENIC
homozygous
139135305
12
34993781
34993782
A
C
8
GENIC
homozygous
139135306
12
34995324
34995325
C
T
20
GENIC
homozygous
139135307
12
34995674
34995675
A
G
21
GENIC
possibly homozygous
139135308
12
34996192
34996196
TTTA
16
GENIC
homozygous
139053607
12
34999827
34999827
CACG
17
GENIC
homozygous
139053608
12
35000019
35000020
G
A
15
GENIC
homozygous
139135309
12
35000262
35000262
TG
16
GENIC
homozygous
139053610
12
35000377
35000378
A
G
16
GENIC
homozygous
139135310
12
35002506
35002507
C
T
21
GENIC
homozygous
139135311
12
35002581
35002582
A
C
20
GENIC
possibly homozygous
139135312
12
35002725
35002726
C
G
19
GENIC
homozygous
139135313
12
35004236
35004236
CAGGTCT
19
GENIC
homozygous
139053611
12
35004315
35004316
G
A
17
GENIC
homozygous
139135314
12
35005654
35005655
G
C
20
GENIC
homozygous
139135315
12
35007942
35007942
CAGCAGGGGTGGATCCGATGCCAGCCTGTGTCTTTCTCACACATAAGC
1
GENIC
homozygous
139053612
12
35008424
35008425
T
C
6
GENIC
homozygous
139135316
12
35008570
35008574
TGAA
14
GENIC
homozygous
139053613
12
35008625
35008626
C
T
13
GENIC
homozygous
139135317
12
35010330
35010331
A
G
9
GENIC
homozygous
139135318
12
35011274
35011275
T
G
13
GENIC
homozygous
139135319
