chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
12
54187778
54187779
G
C
3
GENIC
heterozygous
50260633
12
54188137
54188138
C
T
29
GENIC
homozygous
50260635
12
54188952
54188954
AA
--
1
GENIC
homozygous
50260641
12
54189473
54189474
C
A
3
GENIC
homozygous
50260645
12
54190301
54190302
A
-
2
GENIC
homozygous
50260647
12
54190412
54190413
C
G
16
GENIC
homozygous
50260648
12
54190692
54190693
G
GA
5
GENIC
homozygous
50260650
12
54191358
54191359
C
-
7
GENIC
homozygous
50260654
12
54191901
54191903
TC
--
1
GENIC
homozygous
50260656
12
54192676
54192677
T
C
22
GENIC
homozygous
50260662
12
54193388
54193389
G
A
17
GENIC
homozygous
50260664
12
54194992
54195040
CTGCTTCAGGCTGCTGTGTACTAGCTGTCCTTGTGCCAGGCCCATCCC
------------------------------------------------
7
GENIC
homozygous
50514493
12
54195623
54195624
C
T
14
GENIC
homozygous
50260670
12
54195914
54195915
G
A
17
GENIC
homozygous
50260672
12
54196213
54196214
G
GAATA
5
GENIC
homozygous
50260674
