chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
84572115
84572116
T
C
13
GENIC
possibly homozygous
51722969
10
84572649
84572650
T
G
19
GENIC
homozygous
51722971
10
84573921
84573922
T
C
18
GENIC
homozygous
51722973
10
84574356
84574357
T
C
10
GENIC
homozygous
51523656
10
84574389
84574390
T
C
18
GENIC
homozygous
51722977
10
84574788
84574789
A
C
32
GENIC
homozygous
51722980
10
84574852
84574853
T
C
24
GENIC
possibly homozygous
51722982
10
84574927
84574928
T
C
26
GENIC
possibly homozygous
51722984
10
84575199
84575200
T
C
22
GENIC
homozygous
51722986
10
84575680
84575681
G
A
10
GENIC
homozygous
51722988
10
84576162
84576163
A
C
24
GENIC
possibly homozygous
51722990
10
84577187
84577188
C
T
21
GENIC
homozygous
51722992
10
84577548
84577549
A
G
21
GENIC
heterozygous
51722994
10
84577728
84577729
T
C
27
GENIC
homozygous
51722996
10
84578081
84578082
A
-
6
GENIC
heterozygous
51722998
10
84578109
84578135
CCTGGAGGTTCAACAAGGGAATGTCT
--------------------------
2
GENIC
heterozygous
51722999
10
84578247
84578248
C
T
21
GENIC
possibly homozygous
51723003
10
84578477
84578478
G
T
3
GENIC
homozygous
51723005
10
84578480
84578481
G
A
4
GENIC
homozygous
51723007
