chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
1
85486676
85486676
TTTA
39
GENIC
homozygous
131259496
1
85486764
85486765
C
39
GENIC
homozygous
127399853
1
85486791
85486791
A
44
GENIC
homozygous
127399854
1
85486795
85486795
T
44
GENIC
homozygous
127399855
1
85486847
85486848
G
A
39
GENIC
homozygous
109504702
1
85487826
85487827
A
C
37
GENIC
homozygous
109504703
1
85487875
85487876
C
T
39
GENIC
homozygous
109504704
1
85488386
85488387
T
C
41
GENIC
homozygous
109504705
1
85488671
85488672
C
T
33
GENIC
homozygous
109504706
1
85489402
85489403
C
G
38
GENIC
homozygous
108882177
1
85487414
85487415
C
T
26
GENIC
homozygous
108882175
1
85489443
85489443
TTCT
46
GENIC
homozygous
131259497
1
85490051
85490052
T
C
55
GENIC
homozygous
108882178
1
85490654
85490655
G
T
36
GENIC
homozygous
109504707
1
85490723
85490724
G
A
32
GENIC
homozygous
109504708
1
85493237
85493237
CATTG
39
GENIC
possibly homozygous
131259498
1
85493241
85493241
ATT
39
GENIC
possibly homozygous
131259499
1
85493244
85493244
CCTTGCCA
41
GENIC
possibly homozygous
131259500
1
85493246
85493246
CTGCAGTTTCCCTCTTCGATGGGTGTGGGAAACAAAAAGTGAGAATTCA
40
GENIC
possibly homozygous
131259501
1
85493478
85493478
TC
45
GENIC
homozygous
131259502
1
85492883
85492884
G
A
47
GENIC
homozygous
120868854
