chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
5
165379818
165379818
G
19
GENIC
homozygous
128268818
5
165379823
165379823
A
19
GENIC
homozygous
128268819
5
165379828
165379828
C
19
GENIC
homozygous
128268820
5
165379831
165379831
T
20
GENIC
homozygous
128268821
5
165379834
165379841
ACACGTG
21
GENIC
homozygous
128268822
5
165379863
165379864
G
21
GENIC
homozygous
128268823
5
165380708
165380709
T
15
GENIC
homozygous
128268824
5
165380770
165380771
G
13
GENIC
homozygous
128268825
5
165381957
165381957
GGGGCTGGGG
11
GENIC
possibly homozygous
128268826
5
165383985
165383985
GTGGCCTCTGGCTTGTAGTCCTCCTATGTTAGCTTCCCAAGTGAACCACTAAACTCATCTTTACCTTTGTCCTTTAATGCAAGAGGCCTCTATTAGTCAGGTTTCAGCCTGGAACAAGCCCAGAGCACAATTTTTTTTAAAAGACTTACTCATTTATTATATAT
8
GENIC
homozygous
128268827
5
165387965
165387965
C
11
GENIC
homozygous
128268828
5
165387971
165387972
T
10
GENIC
homozygous
128268829
5
165390990
165390992
CA
20
GENIC
heterozygous
128268830