chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
12
11038298
11038299
A
G
13
GENIC
homozygous
139082976
12
11038955
11038956
G
T
12
GENIC
homozygous
139082977
12
11039013
11039014
T
13
GENIC
homozygous
139040629
12
11039168
11039169
G
A
16
GENIC
homozygous
139082978
12
11039411
11039412
T
A
18
GENIC
homozygous
139082979
12
11043358
11043359
G
A
21
GENIC
homozygous
139082980
12
11044296
11044296
C
32
GENIC
homozygous
139040630
12
11044868
11044869
G
C
27
GENIC
homozygous
139082981
12
11041594
11041594
TTTTTTTT
13
GENIC
heterozygous
147696343
12
11041599
11041599
ATATTTTATTTATTTATTATATATGAG
10
GENIC
heterozygous
147696344
12
11046308
11046309
T
C
33
GENIC
homozygous
139082982
12
11049131
11049132
T
C
18
GENIC
homozygous
139082983
12
11049659
11049659
GCTCA
22
GENIC
homozygous
139040631
12
11050334
11050335
C
T
27
GENIC
homozygous
139082984
12
11050502
11050503
A
T
25
GENIC
homozygous
139082985
12
11050939
11050940
G
A
20
GENIC
homozygous
139082986
12
11052007
11052008
C
T
19
GENIC
homozygous
139082987
12
11052224
11052225
T
G
25
GENIC
homozygous
139082988
12
11052366
11052367
C
G
26
GENIC
homozygous
139082989
12
11052918
11052918
CTGGAACTCAAAGTTTACC
16
GENIC
homozygous
139040632
12
11053841
11053842
C
T
24
GENIC
homozygous
139082990
12
11054299
11054300
C
T
21
GENIC
homozygous
139082991
12
11055870
11055871
C
T
20
GENIC
homozygous
139082992
12
11055975
11055976
G
A
18
GENIC
homozygous
139082993
