chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
18081048
18081049
G
GT
21
GENIC
possibly homozygous
51335556
10
18081101
18081105
TTTT
----
10
GENIC
homozygous
51335557
10
18081457
18081458
T
C
19
GENIC
homozygous
51335558
10
18081938
18081939
C
T
16
GENIC
homozygous
51628938
10
18083089
18083090
G
A
14
GENIC
homozygous
51628939
10
18083677
18083678
G
A
13
GENIC
homozygous
51335561
10
18084726
18084727
T
TCTCACACAAAAGCAAGGGTGCCACCA
24
GENIC
homozygous
52358082
10
18084919
18084920
C
CACAG
15
GENIC
homozygous
51335564
10
18085800
18085801
G
A
10
GENIC
homozygous
51335565
10
18085828
18085829
T
C
9
GENIC
homozygous
51335566
10
18085890
18085891
T
C
13
GENIC
homozygous
51335567
10
18086676
18086677
T
A
17
GENIC
homozygous
51335569
10
18086682
18086683
T
TTGAC
16
GENIC
homozygous
51335570
10
18087263
18087267
TTTT
----
5
GENIC
homozygous
51335571
10
18088224
18088225
A
C
12
GENIC
homozygous
51335572
10
18090136
18090137
C
CA
9
GENIC
heterozygous
52358086
10
18090259
18090260
G
GTTTTTTTTTTTTTTTTGTCTAAAATATTTTTTTTTTATTAACTTGAGTATTTC
1
GENIC
homozygous
52358088
10
18090720
18090721
G
T
15
GENIC
homozygous
51335574
10
18090780
18090781
A
G
19
GENIC
homozygous
51335575
10
18090853
18090854
A
G
25
GENIC
homozygous
51628940
10
18088791
18088792
G
A
17
GENIC
homozygous
51815735
10
18085933
18085934
C
T
21
GENIC
homozygous
51815733