chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
7
11828466
11828467
G
A
30
GENIC
homozygous
53789460
7
11829027
11829028
C
CG
29
GENIC
possibly homozygous
53789462
7
11830455
11830456
T
TCC
8
GENIC
homozygous
54954578
7
11831481
11831527
GTGTGTGTGTGTGCGTGCGTGCGTGTGCGTGTGCGTGTGTGTGTGC
----------------------------------------------
12
GENIC
heterozygous
54954580
7
11832722
11832723
A
T
37
GENIC
homozygous
53789468
7
11833215
11833216
A
AGAGGAC
24
GENIC
homozygous
53789469
7
11833424
11833425
G
GTGT
12
GENIC
heterozygous
54954582
7
11833916
11833917
C
T
37
GENIC
homozygous
53789470
7
11834565
11834566
T
G
35
GENIC
possibly homozygous
53789471
7
11835051
11835052
T
C
25
GENIC
homozygous
53789472
7
11836669
11836670
G
A
29
GENIC
homozygous
53789473
7
11837735
11837736
C
T
46
GENIC
homozygous
53789474
7
11839496
11839497
A
G
30
GENIC
homozygous
53789475
7
11842474
11842475
C
T
39
GENIC
homozygous
53789476
7
11842950
11842951
A
G
24
GENIC
possibly homozygous
53789477
7
11843047
11843073
ATGCTGTCATGTCGTGATGTCATGTG
--------------------------
21
GENIC
homozygous
54884904
7
11843091
11843092
G
A
26
GENIC
homozygous
53789481
7
11843633
11843634
C
A
31
GENIC
homozygous
53789482
7
11843681
11843682
C
T
28
GENIC
homozygous
53789483
