chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
47223028
47223029
T
C
22
GENIC
homozygous
53109231
8
47224230
47224231
C
A
29
GENIC
homozygous
53109232
8
47225455
47225456
G
A
44
GENIC
homozygous
53109233
8
47225494
47225495
A
T
54
GENIC
homozygous
53109234
8
47225749
47225750
G
A
43
GENIC
homozygous
53109235
8
47225816
47225817
A
C
46
GENIC
homozygous
53109236
8
47225823
47225825
TG
--
43
GENIC
homozygous
53109237
8
47225835
47225836
G
A
36
GENIC
homozygous
53381375
8
47225979
47225980
C
CTGTGTG
24
GENIC
heterozygous
53381377
8
47225979
47225980
C
CTGTGTGTG
24
GENIC
possibly homozygous
53381379
8
47226168
47226169
T
TTGTTTTGTTTTGTTTTTTTGTTTTTTTGGTTTTTTTTGG
8
GENIC
homozygous
53381381
8
47226177
47226178
T
C
1
GENIC
homozygous
53109238
8
47226549
47226550
C
T
18
GENIC
homozygous
53381383
8
47226805
47226806
C
A
16
GENIC
homozygous
53109239
8
47227160
47227161
T
C
25
GENIC
homozygous
53109243
8
47227718
47227719
T
TTAGAAACTAAGCTTTCATCGCTTCTCGGCCTTTTGGCTAAGATCAAGTG
31
GENIC
homozygous
53381385
8
47228601
47228602
G
T
31
GENIC
homozygous
53109244
8
47228634
47228635
C
A
20
GENIC
homozygous
53109245
8
47228657
47228658
C
T
21
GENIC
homozygous
53109246
8
47229466
47229467
G
GAGCTCACACTGCAGA
22
GENIC
homozygous
53381387
8
47229814
47229816
CC
--
19
GENIC
homozygous
52970848
