chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
2
115823979
115823980
A
22
GENIC
possibly homozygous
127668439
2
115823989
115823990
A
G
22
GENIC
possibly homozygous
120145241
2
115824550
115824551
T
C
18
GENIC
homozygous
109988497
2
115825124
115825125
T
C
14
GENIC
homozygous
109988498
2
115824086
115824087
T
G
13
GENIC
homozygous
109988495
2
115824266
115824267
C
A
19
GENIC
homozygous
109988496
2
115825206
115825207
T
C
22
GENIC
homozygous
109988499
2
115826412
115826413
C
T
12
GENIC
homozygous
109988500
2
115827770
115827771
A
G
22
GENIC
homozygous
109988501
2
115829763
115829764
T
C
17
GENIC
homozygous
109988502
2
115829796
115829797
C
T
18
GENIC
homozygous
109988503
2
115830105
115830106
C
T
20
GENIC
homozygous
109988504
2
115830485
115830486
G
A
19
GENIC
homozygous
109988505
2
115831318
115831319
C
10
GENIC
homozygous
127668440
2
115831531
115831531
AGGG
11
GENIC
homozygous
127668442
2
115831922
115831950
CCAGCATTTATGTTCGCAGTGCAGGAGA
16
GENIC
homozygous
127668443
2
115833785
115833786
C
T
25
GENIC
homozygous
109988514
2
115830662
115830663
A
G
25
GENIC
homozygous
109988506
2
115830910
115830911
C
A
16
GENIC
homozygous
109988507
2
115831167
115831168
A
T
16
GENIC
possibly homozygous
109988508
2
115831617
115831618
C
T
19
GENIC
homozygous
109988509
2
115831799
115831800
T
C
22
GENIC
homozygous
109988510
2
115832493
115832494
C
T
13
GENIC
homozygous
109988511
2
115832980
115832981
A
G
17
GENIC
homozygous
109988512
2
115833390
115833391
G
A
33
GENIC
homozygous
109988513
2
115834073
115834074
G
A
26
GENIC
homozygous
109988515
2
115834241
115834242
T
C
28
GENIC
homozygous
109988516
2
115835344
115835345
G
C
21
GENIC
homozygous
109988517
2
115835429
115835430
A
G
27
GENIC
homozygous
109988518
2
115835659
115835659
CA
14
GENIC
homozygous
127668444
2
115836095
115836096
A
G
13
GENIC
homozygous
109988519
2
115836821
115836822
C
T
19
GENIC
homozygous
109988520
2
115835856
115835857
A
C
24
GENIC
homozygous
120126439
2
115835857
115835858
G
A
24
GENIC
homozygous
120126440