chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
12
46798522
46798526
AACA
45
GENIC
homozygous
128996730
12
46799526
46799527
T
C
56
GENIC
homozygous
115342551
12
46801416
46801417
G
C
63
GENIC
homozygous
115396992
12
46802661
46802662
A
G
52
GENIC
homozygous
115342553
12
46807417
46807418
C
T
51
GENIC
homozygous
115342557
12
46811877
46811878
T
C
54
GENIC
homozygous
115444205
12
46821658
46821672
CCACCCCACCCCAC
37
GENIC
homozygous
128996731
12
46825042
46825043
C
T
52
GENIC
homozygous
118272499
12
46827878
46827879
T
G
49
GENIC
homozygous
115342559
12
46828324
46828350
TGCATGTGTGCGTGTGTGTGCATGCA
45
GENIC
homozygous
128996732
12
46828624
46828625
T
C
17
GENIC
homozygous
115567677
12
46829121
46829121
TGGA
32
GENIC
possibly homozygous
128996733
12
46831119
46831120
A
G
17
GENIC
homozygous
118272502
12
46831250
46831251
T
C
39
GENIC
homozygous
115397078
12
46831387
46831388
C
T
41
GENIC
homozygous
115342561
12
46831390
46831391
C
G
40
GENIC
homozygous
115342563
12
46832755
46832756
A
42
GENIC
homozygous
128996734
12
46832972
46832973
T
G
45
GENIC
possibly homozygous
115444206
12
46834144
46834145
T
C
24
GENIC
homozygous
115452031
12
46842884
46842885
A
G
51
GENIC
homozygous
115342565
12
46843428
46843429
C
49
GENIC
homozygous
128996735
12
46844860
46844861
G
T
46
GENIC
homozygous
115342567
