chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
1
160494303
160494304
G
A
24
GENIC
homozygous
60916926
1
160494780
160494781
C
A
14
GENIC
homozygous
61547196
1
160496356
160496357
G
A
20
GENIC
homozygous
61547197
1
160497482
160497483
T
C
17
GENIC
homozygous
60916931
1
160498166
160498167
A
C
25
GENIC
homozygous
60916932
1
160498368
160498369
C
G
13
GENIC
homozygous
60916933
1
160500145
160500146
T
G
28
GENIC
homozygous
61547198
1
160502093
160502094
G
GGCAAATTCTA
15
GENIC
homozygous
61547199
1
160502551
160502552
C
T
18
GENIC
homozygous
61547200
1
160503792
160503793
A
C
20
GENIC
homozygous
61547201
1
160506278
160506279
T
C
31
GENIC
homozygous
61547203
1
160506352
160506353
G
A
23
GENIC
homozygous
61547204
1
160506758
160506759
C
CCCA
8
GENIC
homozygous
60916959
1
160510635
160510636
T
C
19
GENIC
homozygous
60916967
1
160501417
160501445
CACACACACACACACACACACACACACA
----------------------------
7
GENIC
possibly homozygous
62555229
1
160510042
160510043
T
C
21
GENIC
homozygous
60916965
1
160511616
160511617
G
A
17
GENIC
homozygous
61547205
1
160512239
160512240
A
G
18
GENIC
homozygous
60916969
1
160513105
160513106
T
C
19
GENIC
homozygous
61547206
1
160513258
160513259
G
A
23
GENIC
homozygous
60916971
1
160513403
160513404
T
TA
18
GENIC
homozygous
60916972
1
160513597
160513598
T
G
12
GENIC
homozygous
61547207
1
160514756
160514757
G
GT
10
GENIC
homozygous
60916974
1
160515334
160515335
A
AATG
19
GENIC
homozygous
60916977
1
160515805
160515809
GTGT
----
14
GENIC
heterozygous
61547208
1
160515807
160515809
GT
--
14
GENIC
possibly homozygous
61547209
1
160516090
160516091
C
T
23
GENIC
homozygous
60916979
1
160516851
160516856
TAAAG
-----
10
GENIC
homozygous
61547210
1
160518677
160518678
G
A
17
GENIC
homozygous
60916983
1
160518701
160518702
T
C
19
GENIC
homozygous
60916984
1
160518907
160518908
T
A
22
GENIC
homozygous
60916986
