chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
53386793
53386794
C
CAGGAGAGAGAGAGAGAGAGAG
11
GENIC
heterozygous
53563003
8
53386793
53386794
C
CAGGAGAGAGAGAGAGAGAG
11
GENIC
possibly homozygous
53431154
8
53386904
53386905
A
-
6
GENIC
homozygous
52632591
8
53386910
53386911
G
-
6
GENIC
homozygous
52632593
8
53386914
53386915
G
-
4
GENIC
homozygous
52632595
8
53386921
53386922
G
-
4
GENIC
homozygous
52632597
8
53387006
53387007
G
-
3
GENIC
homozygous
53387229
8
53387010
53387012
GA
--
1
GENIC
homozygous
53387230
8
53387050
53387052
GG
--
4
GENIC
homozygous
53387233
8
53387060
53387061
C
-
5
GENIC
homozygous
52632605
8
53387062
53387063
C
-
5
GENIC
homozygous
52632607
8
53387067
53387068
C
-
6
GENIC
homozygous
52632609
8
53387069
53387071
GT
--
7
GENIC
homozygous
52632611
8
53387074
53387075
G
-
9
GENIC
homozygous
52632613
8
53387079
53387080
G
-
10
GENIC
homozygous
52632615
8
53387086
53387087
C
-
11
GENIC
homozygous
52632617
8
53387091
53387092
C
-
14
GENIC
homozygous
52632619
8
53387096
53387097
C
-
14
GENIC
homozygous
52632621
8
53387103
53387104
C
-
16
GENIC
homozygous
52632623
8
53387108
53387109
C
-
16
GENIC
homozygous
52632625
8
53387114
53387115
G
-
17
GENIC
homozygous
52632627
8
53387121
53387122
C
-
17
GENIC
homozygous
52632629
8
53387137
53387138
T
-
19
GENIC
homozygous
52632631
8
53387534
53387535
C
T
17
GENIC
homozygous
52632633
8
53388181
53388186
GCCAC
-----
12
GENIC
homozygous
52976369
8
53389242
53389243
T
-
32
GENIC
homozygous
52976370
8
53389329
53389330
A
ACTCCCAGGGAGCAGGAACTGTATTTTAGTCGCCTGTGCATCTCCATCCCTCAGAAGAGCACTGCCATGTCAGGTAGTCACTGACAGGAGGAGGTGAGAAATGAGAATGGCTTAGTCCTTTCTCTGCTG
44
GENIC
homozygous
53387234
8
53389832
53389833
A
G
22
GENIC
homozygous
52632641
8
53390008
53390009
G
A
19
GENIC
homozygous
52632643
8
53390106
53390107
T
TCATCC
21
GENIC
homozygous
52632645
8
53390449
53390450
A
G
25
GENIC
homozygous
52632647
8
53390491
53390492
C
T
21
GENIC
homozygous
52632649
8
53390914
53390915
C
T
7
GENIC
homozygous
52632651
