chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
12
46085914
46085918
TGTG
----
19
GENIC
heterozygous
50545566
12
46085916
46085918
TG
--
19
GENIC
possibly homozygous
50545567
12
46086662
46086663
C
A
32
GENIC
homozygous
50217767
12
46086983
46086984
C
T
24
GENIC
homozygous
50217768
12
46087803
46087804
C
T
24
GENIC
homozygous
50339476
12
46087836
46087837
G
C
23
GENIC
homozygous
50217770
12
46087868
46087869
T
G
15
GENIC
homozygous
50217771
12
46088041
46088042
G
A
15
GENIC
homozygous
50217772
12
46088701
46088713
CCTGCCTGCCTG
------------
1
GENIC
homozygous
50545568
12
46089249
46089250
T
C
16
GENIC
homozygous
50217774
12
46091957
46091958
C
A
20
GENIC
homozygous
50339480
12
46092248
46092298
AGCAGTAAGGCAGAGTTCAATCTGCAGCACACATAAAAAACTCAAGTCCC
--------------------------------------------------
5
GENIC
homozygous
50545569
12
46093070
46093071
T
TACACAC
5
GENIC
heterozygous
50545570
12
46093070
46093071
T
TACACACAC
5
GENIC
heterozygous
50545571
12
46093586
46093587
G
A
15
GENIC
homozygous
50339482
12
46094259
46094260
G
GT
16
GENIC
homozygous
50217777
12
46095796
46095797
A
G
26
GENIC
homozygous
50217778
12
46095908
46095909
C
T
31
GENIC
homozygous
50217779
12
46097627
46097628
T
G
7
GENIC
homozygous
50217781
12
46099561
46099562
G
A
20
GENIC
homozygous
50339484
12
46102468
46102469
C
T
15
GENIC
homozygous
50339486
12
46105340
46105341
G
A
25
GENIC
homozygous
50339488
12
46105372
46105373
G
A
26
GENIC
homozygous
50339490
12
46106274
46106275
C
T
31
GENIC
homozygous
50339492
12
46106576
46106577
C
T
20
GENIC
homozygous
50217785
12
46106756
46106757
T
C
18
GENIC
homozygous
50339494
12
46107105
46107106
G
A
29
GENIC
homozygous
50217787
12
46107541
46107542
G
A
16
GENIC
homozygous
50217789
12
46107797
46107798
A
C
9
GENIC
homozygous
50217790
12
46108328
46108329
G
GCC
2
GENIC
homozygous
50217791
12
46109067
46109068
G
C
6
GENIC
homozygous
50217792
