chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
1
226234166
226234167
C
T
53
GENIC
homozygous
108997771
1
226235600
226235601
T
G
53
GENIC
possibly homozygous
108997772
1
226236732
226236733
C
13
GENIC
homozygous
132539071
1
226236748
226236748
T
17
GENIC
homozygous
132539072
1
226236763
226236763
AGTGCTCCCATCACCAGTACTCCCATCAGT
18
GENIC
homozygous
132539073
1
226238297
226238298
G
A
40
GENIC
homozygous
108997778
1
226238303
226238304
C
A
38
GENIC
homozygous
108997779
1
226238400
226238401
C
T
40
GENIC
homozygous
108997780
1
226238442
226238443
T
C
40
GENIC
homozygous
108997781
1
226240853
226240853
CC
9
GENIC
homozygous
131263671
1
226240856
226240857
T
C
9
GENIC
homozygous
121186504
1
226241337
226241338
G
A
43
GENIC
homozygous
108997782
1
226242219
226242220
G
A
36
GENIC
homozygous
108997783
1
226243650
226243651
G
A
49
GENIC
homozygous
108997784
1
226244462
226244463
T
C
55
GENIC
homozygous
108997785
1
226244840
226244841
G
A
43
GENIC
homozygous
108997786
1
226245036
226245037
C
T
50
GENIC
homozygous
108997787
1
226246596
226246597
C
G
52
GENIC
homozygous
108997788
1
226246778
226246779
A
G
63
GENIC
homozygous
108997789
1
226247118
226247119
C
T
37
GENIC
homozygous
108997790
1
226247466
226247467
G
A
44
GENIC
homozygous
108997791
1
226247793
226247794
T
A
47
GENIC
possibly homozygous
108997792
1
226249091
226249091
A
51
GENIC
homozygous
132539074
1
226242075
226242076
T
C
29
GENIC
possibly homozygous
132556808