chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
108396469
108396470
A
G
17
GENIC
possibly homozygous
51953747
10
108396766
108396767
T
C
10
GENIC
homozygous
51596096
10
108396843
108396844
G
A
17
GENIC
homozygous
51953750
10
108397090
108397091
G
T
23
GENIC
possibly homozygous
51596098
10
108397341
108397342
T
C
18
GENIC
homozygous
51953753
10
108397389
108397390
G
A
23
GENIC
possibly homozygous
51953756
10
108398923
108398924
C
T
9
GENIC
possibly homozygous
51953759
10
108399390
108399391
A
G
13
GENIC
possibly homozygous
51953762
10
108399592
108399593
C
T
15
GENIC
possibly homozygous
51596108
10
108400014
108400015
C
CTCT
2
GENIC
heterozygous
51953766
10
108400065
108400066
C
A
7
GENIC
homozygous
51953772
10
108401486
108401487
T
C
11
GENIC
homozygous
51596116
10
108402283
108402284
A
G
18
GENIC
possibly homozygous
51596118
10
108403425
108403426
G
A
12
GENIC
possibly homozygous
51953778
10
108404773
108404774
G
GGCACATAAACGTGTGTTCCCGTGGACCCGTGCTCACGA
2
GENIC
homozygous
52409529
10
108405663
108405664
T
TC
27
GENIC
possibly homozygous
51596126
10
108407067
108407068
T
G
3
GENIC
heterozygous
52734366
10
108407071
108407072
T
G
3
GENIC
heterozygous
52271553
10
108407075
108407076
T
G
2
GENIC
homozygous
52271555
10
108409222
108409223
A
C
5
GENIC
heterozygous
52409533
10
108409485
108409486
A
G
20
GENIC
homozygous
51596140
10
108411969
108411970
C
CACACACACACACACACACAT
13
GENIC
possibly homozygous
52331695
10
108412067
108412068
C
CT
10
GENIC
homozygous
51596149
10
108412524
108412525
C
T
30
GENIC
possibly homozygous
51596151
10
108412774
108412775
T
C
14
GENIC
possibly homozygous
51596153
10
108407056
108407057
T
-
2
GENIC
heterozygous
52447870