chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
47893518
47893519
C
A
13
GENIC
homozygous
52621321
8
47893918
47893919
C
CTTCCTTCT
13
GENIC
homozygous
53429569
8
47894033
47894034
T
G
11
GENIC
homozygous
52621327
8
47894296
47894297
C
CAGATAGATAGATAGAT
2
GENIC
homozygous
53429571
8
47894347
47894348
A
G
22
GENIC
homozygous
52621334
8
47894568
47894573
AAAAG
-----
15
GENIC
homozygous
52621338
8
47894781
47894782
A
AAGGACATTCTTTTTTTTTTTTTTTTTTGGGTTCTTTTTTTCGGAGCTGGGGATCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC
18
GENIC
heterozygous
53429573
8
47895112
47895113
C
A
14
GENIC
homozygous
52621342
8
47896183
47896184
T
A
21
GENIC
homozygous
52621344
8
47896369
47896370
C
CTCCTTCCTTCCT
14
GENIC
homozygous
53429575
8
47896399
47896402
TTC
---
6
GENIC
homozygous
53799744
8
47896408
47896409
C
-
8
GENIC
possibly homozygous
53799746
8
47896507
47896508
G
T
23
GENIC
homozygous
52621362
8
47896939
47896949
TTGTGTGTGT
----------
1
GENIC
homozygous
53429581
8
47896978
47896984
TGTGTA
------
5
GENIC
heterozygous
53603900
8
47897268
47897269
G
C
11
GENIC
homozygous
52621364
8
47897432
47897433
A
G
9
GENIC
homozygous
52621366
8
47897614
47897615
C
CT
6
GENIC
homozygous
52621374
8
47897679
47897680
T
C
14
GENIC
homozygous
52621376
8
47897711
47897712
C
CTCTTTCTTTCTT
2
GENIC
heterozygous
53382260
8
47897711
47897712
C
CTCTTTCTTTCTTTCTT
2
GENIC
heterozygous
53429583
8
47897775
47897776
C
CTTCCTTCT
7
GENIC
homozygous
53363470
8
47898166
47898170
GTGT
----
7
GENIC
heterozygous
53429585
8
47898168
47898170
GT
--
7
GENIC
heterozygous
53429587
8
47898178
47898182
TGTG
----
4
GENIC
heterozygous
53429591
8
47898709
47898710
C
T
5
GENIC
homozygous
52621382
8
47898730
47898731
C
T
7
GENIC
homozygous
52621384
8
47898794
47898795
G
A
1
GENIC
homozygous
52621386
8
47897586
47897587
C
CTTCCTCCCTCCT
1
GENIC
homozygous
53506777
