chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
12
21486665
21486666
T
-
109
GENIC
heterozygous
50110696
12
21487656
21487657
A
T
57
GENIC
heterozygous
50110721
12
21487699
21487709
ACACACACAC
----------
9
GENIC
heterozygous
50537784
12
21488434
21488435
G
GAT
37
GENIC
heterozygous
50537786
12
21488470
21488471
T
TTTGGAAAGTTC
40
GENIC
heterozygous
50537788
12
21488499
21488500
A
AT
37
GENIC
heterozygous
50110751
12
21488669
21488673
GCCC
----
10
GENIC
heterozygous
50537790
12
21488675
21488676
T
TTGGA
9
GENIC
heterozygous
50537792
12
21491208
21491209
A
ACACG
61
GENIC
possibly homozygous
50110763
12
21491906
21491907
A
C
25
GENIC
homozygous
50110765
12
21493234
21493235
G
A
34
GENIC
homozygous
50110767
12
21488513
21488525
GTGTGTGTGTGT
------------
39
GENIC
heterozygous
50507730
12
21494276
21494277
A
-
12
GENIC
homozygous
50110800
12
21494292
21494293
C
T
14
GENIC
homozygous
50110802
12
21495952
21495953
C
CAA
3
GENIC
homozygous
50110820
12
21495981
21495982
T
TG
5
GENIC
homozygous
50110822
12
21495990
21495991
T
C
8
GENIC
homozygous
50110824
12
21496003
21496004
T
C
9
GENIC
homozygous
50110826
12
21496008
21496009
T
G
9
GENIC
homozygous
50110828
12
21496068
21496069
G
A
18
GENIC
homozygous
50110830
12
21496318
21496319
G
A
14
GENIC
homozygous
50110832
12
21496876
21496877
G
GT
8
GENIC
heterozygous
50110834
12
21496876
21496877
G
GTT
8
GENIC
heterozygous
50557514
12
21497155
21497156
C
CTGTGTGTG
7
GENIC
heterozygous
50537794
12
21497155
21497156
C
CTGTGTGTGTG
7
GENIC
heterozygous
50537797
12
21507629
21507630
T
-
3
GENIC
homozygous
50110846
12
21508194
21508195
T
TTCCCCTCACAGATAGAATAACACAGTACAGATTGATCAA
4
GENIC
homozygous
50537799
12
21508361
21508362
C
CA
53
GENIC
heterozygous
50110864
12
21508399
21508400
T
-
64
GENIC
heterozygous
50110868