chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
13
92595659
92595660
T
TTG
16
GENIC
possibly homozygous
49962816
13
92596220
92596221
C
CGGAAA
12
GENIC
homozygous
50530601
13
92596273
92596275
AA
--
17
GENIC
heterozygous
50893744
13
92597103
92597104
C
A
21
GENIC
homozygous
49962818
13
92600350
92600351
G
GCACACA
9
GENIC
possibly homozygous
50134637
13
92596274
92596275
A
-
17
GENIC
heterozygous
50134633
13
92596881
92596882
A
AG
12
GENIC
homozygous
49859696
13
92596940
92596941
G
A
25
GENIC
homozygous
49859697
13
92597011
92597012
G
A
27
GENIC
homozygous
49859698
13
92597038
92597039
A
G
26
GENIC
homozygous
49859699
13
92597116
92597117
A
C
20
GENIC
homozygous
49859700
13
92597104
92597105
A
G
21
GENIC
homozygous
50497370
13
92600350
92600351
G
GCACA
9
GENIC
heterozygous
50893746
13
92600864
92600865
A
AGGAGAAGGAGGAGAAGGAGGAGGGAGAGGAGGAGGAGAAGGAGGAGGG
5
GENIC
heterozygous
50530603
13
92600903
92600904
T
G
8
GENIC
homozygous
50530605
13
92601476
92601477
G
GGT
20
GENIC
possibly homozygous
49962830
13
92606251
92606252
A
-
15
GENIC
heterozygous
50658679
13
92608693
92608694
A
AGCACAAAAAATGGCAGTTGTT
13
GENIC
homozygous
50530607
13
92619844
92619845
G
GATT
4
GENIC
homozygous
49859711
13
92621906
92621908
TG
--
23
GENIC
heterozygous
50584911
13
92622720
92622721
T
C
9
GENIC
homozygous
49859712
13
92624028
92624029
A
AGT
14
GENIC
heterozygous
50553626
13
92624029
92624031
GT
--
14
GENIC
heterozygous
50553627
13
92627614
92627616
CA
--
10
GENIC
heterozygous
50530614
13
92628084
92628085
C
A
18
GENIC
homozygous
49859713
13
92629614
92629615
C
T
16
GENIC
homozygous
49962906
13
92629615
92629616
T
A
17
GENIC
homozygous
50497376
13
92608264
92608268
GTGT
----
1
GENIC
homozygous
50566407
