chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
108396766
108396767
T
C
20
GENIC
possibly homozygous
51596096
10
108397090
108397091
G
T
5
GENIC
homozygous
51596098
10
108397871
108397872
C
T
21
GENIC
homozygous
51596100
10
108397987
108397988
C
T
16
GENIC
homozygous
51596102
10
108398368
108398369
A
G
12
GENIC
possibly homozygous
51596104
10
108398863
108398864
T
C
19
GENIC
homozygous
51596106
10
108399592
108399593
C
T
20
GENIC
possibly homozygous
51596108
10
108400449
108400450
A
G
24
GENIC
possibly homozygous
51596112
10
108401486
108401487
T
C
11
GENIC
possibly homozygous
51596116
10
108402283
108402284
A
G
23
GENIC
possibly homozygous
51596118
10
108403922
108403924
AA
--
16
GENIC
homozygous
51596124
10
108404773
108404774
G
GGCACATAAACGTGTGTTCCCGTGGACCCGTGCTCACGA
3
GENIC
homozygous
52409529
10
108405663
108405664
T
TC
15
GENIC
homozygous
51596126
10
108407879
108407880
A
T
24
GENIC
possibly homozygous
51596132
10
108409222
108409223
A
C
1
GENIC
homozygous
52409533
10
108409485
108409486
A
G
17
GENIC
homozygous
51596140
10
108410258
108410259
T
A
17
GENIC
possibly homozygous
51596142
10
108411238
108411239
G
A
27
GENIC
possibly homozygous
51596144
10
108412065
108412066
G
A
10
GENIC
possibly homozygous
51596148
10
108412067
108412068
C
CT
8
GENIC
homozygous
51596149
10
108412524
108412525
C
T
20
GENIC
homozygous
51596151
10
108412774
108412775
T
C
24
GENIC
homozygous
51596153
