chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
114705438
114705439
G
A
20
GENIC
homozygous
53166675
8
114705626
114705627
C
T
30
GENIC
homozygous
53166677
8
114706477
114706478
G
A
7
GENIC
homozygous
53166679
8
114707055
114707056
A
G
18
GENIC
homozygous
52824621
8
114707345
114707346
G
T
28
GENIC
homozygous
53166681
8
114707781
114707782
A
G
44
GENIC
homozygous
52824624
8
114708255
114708256
C
T
34
GENIC
homozygous
53166683
8
114708751
114708752
T
TCACCCATGACTGACACCCGGCAC
24
GENIC
homozygous
53367912
8
114708908
114708909
T
C
21
GENIC
homozygous
52824631
8
114708931
114708932
T
C
23
GENIC
homozygous
52824632
8
114710435
114710439
TTTT
----
7
GENIC
heterozygous
52824634
8
114710436
114710439
TTT
---
7
GENIC
possibly homozygous
52824635
8
114711305
114711306
A
G
26
GENIC
homozygous
52824637
8
114711504
114711505
T
TAC
15
GENIC
homozygous
52824638
8
114711506
114711507
T
TACATAC
11
GENIC
homozygous
53523438
8
114711511
114711512
G
GGAGAGAGA
10
GENIC
heterozygous
53410945
8
114711719
114711720
C
CT
31
GENIC
homozygous
52824641
8
114711962
114711963
A
G
17
GENIC
homozygous
53166693
8
114712192
114712193
A
G
22
GENIC
homozygous
53166695
8
114712197
114712199
TT
--
21
GENIC
homozygous
53166697
8
114712386
114712387
T
TA
12
GENIC
homozygous
53166699
8
114712395
114712396
T
C
13
GENIC
homozygous
53166701
8
114713870
114713871
A
ATCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC
10
GENIC
homozygous
53410946
8
114714285
114714286
C
-
21
GENIC
homozygous
53166703
8
114714484
114714485
G
GA
7
GENIC
heterozygous
53410947
8
114714485
114714486
A
-
7
GENIC
heterozygous
53410948
8
114714565
114714566
T
G
17
GENIC
homozygous
53166705
8
114714641
114714642
A
G
20
GENIC
homozygous
53166707
8
114715206
114715207
C
A
27
GENIC
homozygous
53166709
8
114715664
114715688
TGTGTGTGTGTGTGTGTGTGTGTG
------------------------
23
GENIC
homozygous
52824644
8
114716555
114716556
G
A
20
GENIC
homozygous
53166711
8
114717697
114717698
G
A
24
GENIC
homozygous
53166713
