chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
17
53092493
53092494
C
T
27
GENIC
homozygous
47327804
17
53093095
53093096
T
G
32
GENIC
homozygous
47132483
17
53093150
53093151
T
G
29
GENIC
homozygous
47132484
17
53093152
53093153
A
G
30
GENIC
homozygous
47132485
17
53093208
53093209
G
C
28
GENIC
homozygous
47132486
17
53093515
53093517
GT
--
27
GENIC
homozygous
47132487
17
53093629
53093630
T
TA
38
GENIC
homozygous
47132488
17
53093663
53093664
C
T
38
GENIC
homozygous
47132489
17
53093765
53093766
T
C
22
GENIC
homozygous
47132490
17
53093901
53093902
A
G
22
GENIC
homozygous
47132491
17
53094404
53094405
A
T
41
GENIC
homozygous
47132492
17
53094453
53094454
A
G
39
GENIC
homozygous
47132493
17
53094456
53094457
G
A
41
GENIC
homozygous
47132494
17
53094690
53094691
C
CA
12
GENIC
homozygous
47132495
17
53095395
53095396
A
AT
19
GENIC
homozygous
47132498
17
53099289
53099290
G
C
21
GENIC
homozygous
47327808
17
53099582
53099583
T
A
10
GENIC
homozygous
47132506
17
53099611
53099614
GGG
---
7
GENIC
homozygous
47132507
17
53099754
53099774
ATGTAAGTCCTTAGTTCTAC
--------------------
16
GENIC
homozygous
47327810
17
53101084
53101085
G
A
37
GENIC
homozygous
47327812
17
53101143
53101144
A
C
34
GENIC
homozygous
47327814
17
53101153
53101154
A
C
30
GENIC
homozygous
47327816
17
53101308
53101309
G
A
28
GENIC
homozygous
47132516
17
53101318
53101319
C
T
25
GENIC
homozygous
47327818
17
53101373
53101374
C
G
22
GENIC
homozygous
47327820
17
53101391
53101392
G
A
21
GENIC
homozygous
47327822
17
53102071
53102072
G
T
40
GENIC
homozygous
47327824
17
53099626
53099627
A
G
11
GENIC
homozygous
47709925
17
53100569
53100570
T
TGAGAGA
7
GENIC
homozygous
47742832
17
53102295
53102296
C
CGTGT
24
GENIC
homozygous
47742838
17
53102236
53102237
A
ATGTGTGCGTG
22
GENIC
homozygous
47809728
17
53102282
53102283
G
GCGTGTGTGT
21
GENIC
homozygous
47809730
17
53102301
53102302
C
CATGTGTGTGTGCATATGTGTGTGCATGTGTGT
11
GENIC
homozygous
47809732