chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
9
95188461
95188462
C
T
12
GENIC
homozygous
52056468
9
95188487
95188488
T
-
10
GENIC
homozygous
52281374
9
95188739
95188740
T
C
18
GENIC
homozygous
52056471
9
95189670
95189671
A
G
28
GENIC
homozygous
52056473
9
95189943
95189944
A
C
17
GENIC
homozygous
52056475
9
95190174
95190175
T
A
25
GENIC
homozygous
52281375
9
95190434
95190435
G
A
12
GENIC
homozygous
52281376
9
95190557
95190558
C
CTT
11
GENIC
heterozygous
52056477
9
95190557
95190558
C
CT
11
GENIC
heterozygous
52955474
9
95190557
95190558
C
CTTT
11
GENIC
heterozygous
53145099
9
95190768
95190769
G
C
21
GENIC
homozygous
52281377
9
95193762
95193763
T
TTC
7
GENIC
heterozygous
52056481
9
95194895
95194896
C
CAG
15
GENIC
homozygous
52056486
9
95194960
95194984
ACACACAGAGAGAGAGAGAGAGAG
------------------------
5
GENIC
heterozygous
52915757
9
95195170
95195171
A
T
14
GENIC
homozygous
52056492
9
95195422
95195423
A
T
19
GENIC
homozygous
52056494
9
95197102
95197103
T
TTCTC
4
GENIC
heterozygous
52955476
9
95197148
95197149
A
ATCTCTC
3
GENIC
heterozygous
52915758
9
95198470
95198471
A
AAAAACAAAAC
15
GENIC
homozygous
53535037
9
95200402
95200403
C
T
13
GENIC
homozygous
52281380
9
95200708
95200709
T
A
12
GENIC
homozygous
52056506
9
95201597
95201598
C
T
6
GENIC
homozygous
52281381
9
95201765
95201837
CTCCCTCCCTCTTAGAGATGCCTTCTGACACACACAAGAGGGCTAGTCACATGAATTTACATCTGAACTGTA
------------------------------------------------------------------------
2
GENIC
homozygous
52915762
9
95202948
95202949
T
C
29
GENIC
homozygous
52056516
9
95202996
95202998
CA
--
23
GENIC
heterozygous
53114123
9
95203464
95203465
G
A
9
GENIC
homozygous
52281382
9
95205135
95205136
A
G
12
GENIC
homozygous
52281383
9
95205240
95205241
C
CCATAT
9
GENIC
homozygous
52056518
9
95205553
95205554
T
TCA
27
GENIC
homozygous
52056522
9
95205557
95205558
C
CAT
27
GENIC
homozygous
52056524
9
95207367
95207368
C
T
21
GENIC
homozygous
52281384