chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
103638773
103638774
A
AT
26
GENIC
homozygous
53158321
8
103640560
103640561
T
C
35
GENIC
homozygous
53158323
8
103640702
103640703
T
A
12
GENIC
homozygous
53158325
8
103640832
103640833
C
T
20
GENIC
homozygous
53158327
8
103642131
103642132
C
CCACAGTCCTGCTGCCTCTGCTTTGCCCA
43
GENIC
homozygous
53652694
8
103642233
103642242
CTGATGGCA
---------
36
GENIC
homozygous
53158331
8
103642324
103642325
T
C
30
GENIC
homozygous
52779352
8
103643662
103643666
AAAA
----
3
GENIC
homozygous
53406400
8
103643880
103643881
T
TTG
23
GENIC
heterozygous
53158335
8
103643923
103643924
A
AGCGTGCGT
34
GENIC
possibly homozygous
53630508
8
103645158
103645159
G
C
19
GENIC
homozygous
52779363
8
103646566
103646567
C
CCAT
8
GENIC
possibly homozygous
53652695
8
103646580
103646581
T
TTCCA
10
GENIC
heterozygous
53652696
8
103647563
103647564
C
T
16
GENIC
homozygous
52779372
8
103648546
103648552
AAAAAA
------
7
GENIC
homozygous
53158343
8
103649109
103649110
A
-
10
GENIC
homozygous
53023222
8
103649126
103649127
T
C
14
GENIC
homozygous
52779376
8
103650132
103650133
C
CA
16
GENIC
heterozygous
53669250
8
103650934
103650935
T
TAAA
10
GENIC
homozygous
53158345
8
103656654
103656659
ACAAA
-----
5
GENIC
homozygous
53158347
8
103656939
103656940
A
T
10
GENIC
homozygous
52779384
8
103657307
103657308
A
G
23
GENIC
homozygous
52779387
8
103657336
103657337
C
T
16
GENIC
homozygous
53158349
8
103657571
103657572
C
CAA
3
GENIC
heterozygous
53158353
8
103658507
103658508
C
T
17
GENIC
homozygous
53367103
8
103658508
103658509
T
G
18
GENIC
homozygous
52779393
8
103661198
103661199
T
C
22
GENIC
homozygous
52779399
8
103661755
103661756
A
-
15
GENIC
possibly homozygous
53158355
