chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
5
81150785
81150786
C
T
19
GENIC
possibly homozygous
55492658
5
81151510
81151511
C
CTGTATGG
3
GENIC
homozygous
55492660
5
81152765
81152766
T
C
11
GENIC
homozygous
55492662
5
81153077
81153078
C
A
2
GENIC
heterozygous
55492664
5
81154508
81154509
G
A
9
GENIC
homozygous
55492666
5
81155187
81155188
A
G
7
GENIC
homozygous
55492668
5
81155608
81155609
A
G
15
GENIC
possibly homozygous
55492670
5
81156672
81156673
A
G
12
GENIC
homozygous
55492672
5
81158316
81158317
C
T
15
GENIC
homozygous
55492674
5
81158685
81158686
C
A
6
GENIC
homozygous
55492676
5
81158707
81158711
CTTG
----
1
GENIC
homozygous
55492678
5
81159234
81159235
A
C
10
GENIC
homozygous
55492680
5
81159619
81159620
C
T
6
GENIC
homozygous
55492682
5
81160859
81160889
AAACCAAACCAAACCAAACCAAACCAAACC
------------------------------
2
GENIC
homozygous
56428914
5
81161297
81161298
A
AT
5
GENIC
homozygous
55492688
5
81161660
81161661
A
G
13
GENIC
homozygous
55492690
