chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
53595888
53595889
T
C
24
GENIC
homozygous
116887332
10
53596200
53596201
T
C
15
GENIC
homozygous
116887334
10
53596336
53596346
AAAACAAAAC
21
GENIC
homozygous
131093790
10
53597930
53597931
T
C
22
GENIC
homozygous
116887336
10
53599351
53599355
TGTT
13
GENIC
homozygous
131093791
10
53600029
53600030
T
C
16
GENIC
homozygous
116887338
10
53600073
53600074
A
G
17
GENIC
homozygous
116887340
10
53600376
53600377
G
C
14
GENIC
homozygous
116887342
10
53600746
53600747
A
11
GENIC
homozygous
131093792
10
53600748
53600860
CTTCGATTTCTTTTTTTTTTTTTGTTCTTTTTTTCGGAGCTGGGGGCCAAACCCAGGGCCTTCCGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCCACA
12
GENIC
homozygous
131093793
10
53601045
53601046
T
19
GENIC
homozygous
131093794
10
53601096
53601097
C
T
21
GENIC
homozygous
116887344
10
53601524
53601525
T
C
23
GENIC
homozygous
116887346
10
53602896
53602897
T
C
15
GENIC
homozygous
116887348
10
53603902
53603903
A
G
24
GENIC
homozygous
116887350
10
53604160
53604161
A
G
15
GENIC
homozygous
116887352
10
53604263
53604263
T
15
GENIC
homozygous
131093795
10
53604349
53604350
A
G
15
GENIC
homozygous
116887354
10
53604896
53604897
G
A
18
GENIC
homozygous
116887356
10
53605006
53605007
C
A
20
GENIC
homozygous
116887358
10
53605117
53605118
T
C
20
GENIC
homozygous
116887360
10
53605274
53605275
T
C
13
GENIC
homozygous
116887362
10
53605952
53605953
A
G
22
GENIC
homozygous
116887364
10
53606461
53606462
A
G
13
GENIC
homozygous
116887366
10
53606719
53606720
C
T
16
GENIC
homozygous
116887368
10
53607446
53607447
A
G
21
GENIC
homozygous
116887370
10
53608104
53608105
C
G
18
GENIC
homozygous
116933687
10
53608437
53608438
A
G
11
GENIC
homozygous
116887372
10
53603143
53603144
G
C
7
GENIC
homozygous
117344656
