chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
1
257868592
257868593
T
C
13
GENIC
homozygous
135879133
1
257872843
257872844
A
G
32
GENIC
homozygous
135879134
1
257873308
257873309
G
A
33
GENIC
homozygous
135879135
1
257876808
257876809
T
C
10
GENIC
homozygous
135879136
1
257877292
257877293
C
T
22
GENIC
homozygous
135879137
1
257874619
257874619
GGTGCATGTGTATATAGGTGTTCATGGGGTGTATGTGTAGGGGTACGTGTGTGTAGGAGTGCATGTGTGTGTAGA
11
GENIC
homozygous
135475848
1
257876646
257876767
ACTTTCTATTCACTCAAAAGGGCTTGGGTGGCCTCTATGCAAATATTAAAGCTATACGTCTGGACTTTGATCGCTCCATCAGCAATGGAGAGTAGTTAAGGCCAGGTCAAGAGGTTTGTAT
12
GENIC
homozygous
135475849
1
257878108
257878110
TC
17
GENIC
homozygous
135475850
1
257878280
257878282
GT
22
GENIC
homozygous
135475851
1
257878284
257878285
T
C
24
GENIC
homozygous
135879138
1
257878286
257878287
C
25
GENIC
homozygous
135475852
1
257878299
257878300
C
T
22
GENIC
homozygous
135879139
1
257878999
257879000
G
23
GENIC
homozygous
135475853
1
257879125
257879126
C
G
46
GENIC
homozygous
135879140
1
257879899
257879900
A
G
21
GENIC
homozygous
135879141
1
257880566
257880567
A
G
35
GENIC
homozygous
135879142
1
257881599
257881600
C
T
14
GENIC
homozygous
135879143
1
257883048
257883049
C
A
28
GENIC
homozygous
135879144