chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
7
91518986
91518987
T
C
24
GENIC
homozygous
115760115
7
91519024
91519025
G
A
24
GENIC
homozygous
116050554
7
91520734
91520735
A
G
17
GENIC
homozygous
116050556
7
91523834
91523835
C
T
17
GENIC
homozygous
116050558
7
91524455
91524456
A
G
27
GENIC
homozygous
115760121
7
91526635
91526636
A
G
22
GENIC
homozygous
115760125
7
91527729
91527730
T
C
18
GENIC
homozygous
116050560
7
91528738
91528739
A
23
GENIC
homozygous
128493300
7
91528980
91528980
T
22
GENIC
homozygous
128493301
7
91533735
91533736
T
C
24
GENIC
homozygous
115760143
7
91533901
91533902
T
C
29
GENIC
homozygous
115760145
7
91534555
91534555
TAGTGTATAAGCAAACCTAGCGAAT
20
GENIC
homozygous
128493303
7
91535566
91535567
A
G
24
GENIC
homozygous
115760151
7
91536367
91536368
C
G
20
GENIC
homozygous
116050564
7
91536717
91536718
C
T
35
GENIC
homozygous
116050566
7
91537884
91537885
C
A
18
GENIC
homozygous
116050568
7
91537979
91537980
A
G
22
GENIC
homozygous
116050570
7
91537992
91537993
C
T
21
GENIC
homozygous
116050573
7
91538179
91538180
T
C
21
GENIC
homozygous
116050575
7
91538548
91538549
G
A
10
GENIC
homozygous
116050577
7
91535014
91535014
A
18
GENIC
homozygous
131020981
7
91536044
91536044
A
22
GENIC
homozygous
131020982
7
91536803
91536803
CTC
22
GENIC
homozygous
131020983
7
91537809
91537809
A
25
GENIC
homozygous
131020984