chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
18
15757636
15757637
T
C
32
GENIC
homozygous
46368280
18
15758831
15758832
C
A
21
GENIC
homozygous
46575599
18
15761303
15761304
G
A
21
GENIC
homozygous
46575600
18
15762245
15762249
TGTG
----
2
GENIC
heterozygous
46809867
18
15762247
15762249
TG
--
2
GENIC
heterozygous
46809868
18
15762295
15762296
A
AT
10
GENIC
homozygous
46368286
18
15762500
15762501
A
G
26
GENIC
homozygous
46575601
18
15764790
15764791
A
AAAAC
18
GENIC
homozygous
46575602
18
15765356
15765357
A
G
20
GENIC
homozygous
46368290
18
15765540
15765541
T
C
9
GENIC
homozygous
46368291
18
15765614
15765615
T
TGA
7
GENIC
homozygous
46575604
18
15766493
15766494
A
G
24
GENIC
homozygous
46368294
18
15767035
15767036
G
GCATGCATGCCTGAGCACACACATGCATGCACGCACGAGCACACACA
23
GENIC
homozygous
46809869
18
15768189
15768190
G
A
34
GENIC
homozygous
46575605
18
15769342
15769343
G
A
27
GENIC
homozygous
46575606
18
15770438
15770440
AA
--
14
GENIC
heterozygous
46368301
18
15770439
15770440
A
-
14
GENIC
possibly homozygous
46575607
18
15771398
15771399
A
T
24
GENIC
homozygous
46575608
18
15771409
15771410
C
T
26
GENIC
homozygous
46368304
