chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
88623448
88623449
C
G
30
GENIC
homozygous
116950078
10
88623754
88623755
C
T
23
GENIC
homozygous
116950080
10
88624100
88624101
G
A
24
GENIC
homozygous
116950082
10
88624284
88624285
G
A
26
GENIC
homozygous
116674243
10
88626632
88626633
A
G
17
GENIC
homozygous
116819127
10
88628407
88628408
T
C
21
GENIC
homozygous
116674245
10
88628742
88628743
A
G
28
GENIC
homozygous
116674247
10
88629167
88629168
T
C
23
GENIC
homozygous
116674249
10
88630525
88630526
C
T
17
GENIC
homozygous
116950084
10
88630880
88630881
C
T
16
GENIC
homozygous
116950086
10
88632408
88632409
A
C
24
GENIC
homozygous
116674255
10
88632450
88632451
A
G
26
GENIC
homozygous
116674257
10
88632760
88632761
G
A
23
GENIC
homozygous
116950088
10
88633796
88633797
G
A
31
GENIC
homozygous
116674261
10
88636068
88636069
G
A
31
GENIC
homozygous
116674265
10
88637143
88637143
AGCAGCAGC
14
GENIC
homozygous
132693765
10
88635410
88635424
TTTTTTTTTTTTCC
19
GENIC
homozygous
132693762
10
88636390
88636390
G
16
GENIC
homozygous
132693763
10
88636391
88636391
TTTGTTG
16
GENIC
homozygous
132693764
10
88637553
88637556
CTT
12
GENIC
homozygous
132693766
10
88637759
88637759
ATGACAAAACCAGAGTTGAGTTCCTTTTAA
13
GENIC
homozygous
128843437
10
88638171
88638172
T
C
26
GENIC
homozygous
116674267
10
88639084
88639085
C
T
28
GENIC
homozygous
116950090
10
88639613
88639613
GC
15
GENIC
homozygous
132693767
10
88640725
88640726
T
C
26
GENIC
homozygous
116674271
10
88640744
88640745
G
T
26
GENIC
homozygous
116950092
10
88641217
88641217
GG
16
GENIC
homozygous
132693768
10
88641420
88641421
C
A
9
GENIC
homozygous
132697248
10
88641425
88641425
C
11
GENIC
homozygous
132693769
10
88643604
88643605
G
A
11
GENIC
homozygous
116950094
10
88643780
88643781
C
A
20
GENIC
homozygous
116950096
10
88643799
88643800
G
A
20
GENIC
homozygous
116950098
10
88643976
88643977
T
C
14
GENIC
homozygous
116950100
10
88645127
88645128
A
G
10
GENIC
homozygous
116674279
10
88639610
88639611
C
T
18
GENIC
homozygous
116982462
