chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
96940222
96940223
T
C
29
GENIC
homozygous
52745589
8
96940235
96940236
G
A
37
GENIC
homozygous
52745590
8
96941817
96941818
C
T
28
GENIC
homozygous
52745591
8
96942261
96942262
A
T
20
GENIC
homozygous
52745592
8
96942346
96942347
G
GTT
20
GENIC
homozygous
52745593
8
96942798
96942799
T
G
34
GENIC
homozygous
52745594
8
96943110
96943111
T
TA
33
GENIC
homozygous
52745595
8
96943559
96943560
C
T
17
GENIC
homozygous
52745596
8
96943816
96943817
C
T
21
GENIC
possibly homozygous
52745597
8
96943855
96943856
C
T
27
GENIC
homozygous
52745598
8
96943856
96943857
A
G
27
GENIC
homozygous
52745599
8
96944032
96944038
ATCCCC
------
19
GENIC
homozygous
53404988
8
96944039
96944040
T
TGGGG
20
GENIC
homozygous
53404989
8
96946383
96946384
A
G
34
GENIC
homozygous
52745602
8
96946677
96946678
C
T
26
GENIC
homozygous
52745603
8
96947914
96947926
TGTCTGTGTGTC
------------
13
GENIC
heterozygous
53404990
8
96947916
96947926
TCTGTGTGTC
----------
10
GENIC
heterozygous
53404991
8
96948460
96948461
T
C
26
GENIC
homozygous
52745605
8
96948518
96948519
G
GA
21
GENIC
possibly homozygous
52745606
8
96950985
96950986
G
GTGGT
23
GENIC
homozygous
52745607
8
96951059
96951060
G
A
50
GENIC
homozygous
52745608
8
96951257
96951258
C
T
39
GENIC
homozygous
52745609
8
96952166
96952167
G
A
33
GENIC
possibly homozygous
52745610
8
96952342
96952343
C
CG
39
GENIC
homozygous
52745611
8
96953230
96953231
C
CCAACCACAGACCAAA
19
GENIC
homozygous
53366569
8
96954778
96954779
A
G
41
GENIC
homozygous
52745612
8
96955076
96955077
C
CACCACAACAACAACA
5
GENIC
homozygous
53520353
8
96955816
96955819
AAC
---
15
GENIC
homozygous
53404993
8
96956404
96956405
T
-
14
GENIC
homozygous
52745616
8
96957216
96957217
T
-
27
GENIC
possibly homozygous
53010447
8
96957887
96957929
TAGCAAGACCCCCTCATAAGATCCCAGGTCCCAACGAGTCTG
------------------------------------------
16
GENIC
homozygous
52745617
8
96958388
96958389
C
G
23
GENIC
homozygous
52745618
