chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
19
36956390
36956391
T
TA
12
GENIC
homozygous
46109861
19
36956921
36956922
A
AAGACAGACTGACAGGCAAGACAGACAGAC
28
GENIC
homozygous
46380061
19
36957156
36957157
G
GT
14
GENIC
possibly homozygous
46109863
19
36957481
36957482
A
-
22
GENIC
homozygous
46109864
19
36959068
36959069
G
A
13
GENIC
homozygous
46109865
19
36959832
36959834
AA
--
15
GENIC
homozygous
46109866
19
36959880
36959881
C
CAG
2
GENIC
heterozygous
46109867
19
36961178
36961179
C
CA
9
GENIC
heterozygous
46249551
19
36961329
36961330
T
G
43
GENIC
homozygous
46109868
19
36963860
36963861
C
T
35
GENIC
homozygous
46109869
19
36967611
36967612
C
G
44
GENIC
homozygous
46109870
19
36970303
36970304
G
A
33
GENIC
homozygous
46109873
19
36970597
36970598
A
AT
31
GENIC
homozygous
46109874
19
36971204
36971205
T
A
33
GENIC
homozygous
46109875
19
36971707
36971708
C
T
38
GENIC
homozygous
46109876
19
36972313
36972314
G
A
43
GENIC
homozygous
46109877
19
36972955
36972956
C
T
38
GENIC
homozygous
46109878
19
36973528
36973531
TTT
---
11
GENIC
heterozygous
46380065
19
36973529
36973531
TT
--
11
GENIC
heterozygous
46520004
19
36975007
36975012
TTATT
-----
24
GENIC
heterozygous
46109880
19
36975008
36975012
TATT
----
24
GENIC
heterozygous
46109881
19
36976220
36976221
A
G
18
GENIC
homozygous
46109882
19
36965118
36965119
C
CT
20
GENIC
heterozygous
46634845
19
36969170
36969175
TTTTT
-----
13
GENIC
heterozygous
46461431
