chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
12
45821636
45821637
T
C
20
GENIC
homozygous
139152565
12
45822814
45822815
A
G
19
GENIC
homozygous
139152566
12
45823129
45823130
A
G
23
GENIC
homozygous
139152567
12
45823622
45823748
GAAATCCACAAGATCGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAGAACCAAAAAAAAAAAAAAAAAAAAAAAA
3
GENIC
homozygous
144914811
12
45824294
45824295
C
A
23
GENIC
homozygous
139152568
12
45824379
45824380
G
C
17
GENIC
homozygous
139152569
12
45825487
45825488
T
C
20
GENIC
homozygous
139152570
12
45825520
45825521
G
A
20
GENIC
possibly homozygous
139152571
12
45825704
45825705
G
A
15
GENIC
homozygous
139152572
12
45826292
45826293
T
C
21
GENIC
homozygous
139152573
12
45826764
45826765
T
C
7
GENIC
homozygous
139152574
12
45827016
45827017
G
A
21
GENIC
homozygous
139152575
12
45827401
45827402
G
A
16
GENIC
homozygous
139152576
12
45828127
45828128
A
G
16
GENIC
homozygous
139152577
12
45828841
45828842
A
G
7
GENIC
homozygous
139152578
12
45828930
45828931
A
C
11
GENIC
homozygous
139152579
12
45828931
45828932
A
G
11
GENIC
homozygous
139152580
12
45829003
45829004
A
G
12
GENIC
homozygous
139152581
12
45829025
45829025
GCTAT
10
GENIC
homozygous
139058879
12
45823782
45823783
T
11
GENIC
homozygous
403327752
12
45823782
45823783
T
G
11
GENIC
heterozygous
403327753
12
45823788
45823789
T
11
GENIC
homozygous
403327754
12
45823788
45823789
T
G
11
GENIC
heterozygous
403327755
12
45823777
45823807
CTCTCTCTCTCTCTCTCGCTCTCGCTCTCG
11
GENIC
homozygous
139058876
12
45823829
45823835
CACACA
13
GENIC
homozygous
139058877
12
45826675
45826675
CCTTCTG
11
GENIC
homozygous
139058878
12
45829121
45829134
CCTAGCAAGCGCA
15
GENIC
homozygous
139058880
12
45829205
45829206
T
G
20
GENIC
homozygous
139152582
12
45830327
45830328
G
A
25
GENIC
homozygous
139152583
12
45830373
45830374
G
A
21
GENIC
homozygous
139152584
12
45830879
45830880
G
A
16
GENIC
homozygous
139152585
12
45831342
45831343
A
G
13
GENIC
homozygous
139152586
