chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
51094502
51094503
C
A
33
GENIC
homozygous
146865573
8
51095726
51095727
T
C
38
GENIC
homozygous
146865574
8
51097626
51097627
T
C
34
GENIC
heterozygous
154520638
8
51097637
51097638
G
A
34
GENIC
heterozygous
154520640
8
51097995
51097996
C
A
39
GENIC
homozygous
138329796
8
51098224
51098225
T
C
32
GENIC
homozygous
138329797
8
51098780
51098781
C
T
28
GENIC
homozygous
138329798
8
51097616
51097727
AAGCGCAAGGTCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAGAACCAAAAAAAAAAAAATTAATGACTTGGGGTTGGGGATTTAGCTCAGCGGTAGAGCGTTTGCCTAGC
34
GENIC
homozygous
146843198
8
51098286
51098403
AAGATACAGACATACTCGGGGTTGGGGATTTGGCTCAGTGGTAGAGCGTTTGCCTAGGAAGCGCAAGGTCCTGGGTTCGGTCCCCAGCCCTGAAAAAAAGAAAAAAGAAAAAAAAAA
26
GENIC
homozygous
138244902
8
51098700
51098701
T
37
GENIC
homozygous
142023745
8
51097620
51097621
G
34
GENIC
homozygous
404007008
8
51097620
51097621
G
A
34
GENIC
heterozygous
404007009
8
51097626
51097627
T
34
GENIC
homozygous
403237584
8
51097637
51097638
G
34
GENIC
homozygous
403237585
