chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
103707111
103707112
A
53
GENIC
homozygous
128623566
8
103715831
103715832
A
G
28
GENIC
homozygous
116618726
8
103732682
103732683
C
A
5
GENIC
homozygous
116618788
8
103740775
103740776
G
A
45
GENIC
heterozygous
128665420
8
103740914
103740915
T
C
37
GENIC
heterozygous
128665421
8
103741525
103741525
TGTT
41
GENIC
homozygous
128623589
8
103750441
103750441
T
39
GENIC
homozygous
128623592
8
103750450
103750451
A
41
GENIC
homozygous
128623593
8
103750516
103750516
C
35
GENIC
homozygous
128623594
8
103750744
103750744
CCATGGGGCTGGGGATTTAGCGCAGTGGTAGAGCGCTTGCCTAGGAAGCTCAAGGCC
22
GENIC
homozygous
128623595
8
103750893
103750894
A
G
50
GENIC
homozygous
116618843
8
103758334
103758335
T
28
GENIC
homozygous
128623597
8
103766110
103766111
T
C
15
GENIC
homozygous
116984560
8
103766113
103766114
T
C
15
GENIC
homozygous
116984561
8
103739843
103739844
T
C
8
GENIC
possibly homozygous
131061066
