chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
15
42489656
42489657
G
A
58
GENIC
homozygous
112493634
15
42489900
42489901
A
G
42
GENIC
homozygous
112493636
15
42490882
42490883
T
G
55
GENIC
homozygous
112493638
15
42491180
42491181
A
G
38
GENIC
homozygous
112493640
15
42491288
42491289
C
T
25
GENIC
homozygous
112493642
15
42491299
42491300
T
C
23
GENIC
homozygous
112493644
15
42491356
42491358
CT
9
GENIC
possibly homozygous
129250619
15
42491594
42491595
G
A
41
GENIC
homozygous
112493646
15
42491610
42491611
C
T
39
GENIC
homozygous
112493648
15
42491690
42491691
T
C
37
GENIC
homozygous
112493650
15
42492819
42492820
A
T
52
GENIC
homozygous
112493652
15
42492820
42492821
A
T
52
GENIC
homozygous
112493654
15
42492838
42492839
T
C
54
GENIC
homozygous
112493656
15
42492958
42492959
C
T
43
GENIC
homozygous
112493658
15
42492989
42492990
T
C
51
GENIC
homozygous
112493660
15
42493048
42493049
A
G
48
GENIC
homozygous
112493662
15
42493344
42493345
A
C
61
GENIC
homozygous
112493664
15
42493623
42493623
G
18
GENIC
homozygous
129250620
15
42494680
42494681
T
C
32
GENIC
homozygous
112493666
15
42495130
42495131
G
A
40
GENIC
homozygous
112493668
15
42495431
42495432
C
T
42
GENIC
homozygous
112493670
15
42495725
42495726
T
G
60
GENIC
homozygous
112493672
15
42495793
42495794
C
T
53
GENIC
homozygous
112493674
15
42496769
42496769
T
47
GENIC
homozygous
129250621
15
42498304
42498304
A
42
GENIC
possibly homozygous
129250622
15
42498619
42498742
CCTGCCTCTTCCTCTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTTTTTTCGGAGCTGGGGACCGAACCCCGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCC
16
GENIC
possibly homozygous
129250623
15
42497147
42497148
C
T
45
GENIC
homozygous
112493676
15
42497655
42497656
A
G
43
GENIC
homozygous
112493678
15
42497939
42497940
G
A
39
GENIC
homozygous
112493680
15
42498419
42498420
A
G
52
GENIC
homozygous
112493682
15
42498442
42498443
G
A
53
GENIC
homozygous
112493684
15
42499198
42499199
T
C
63
GENIC
homozygous
112493686
