chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
7
8184853
8184854
T
C
22
GENIC
homozygous
137998264
7
8185015
8185015
G
22
GENIC
homozygous
137934266
7
8185525
8185526
G
A
15
GENIC
homozygous
137998265
7
8186478
8186479
C
A
19
GENIC
homozygous
137998266
7
8187948
8188028
TGGATGGATGGATGAGTAGATGGATGGGTGAATGGATGGGTGGGTGGGTGGGTGGATGGATGAGTAGATGGATGGGTGGA
12
GENIC
homozygous
137934267
7
8189049
8189049
T
20
GENIC
homozygous
137934268
7
8189291
8189292
A
T
17
GENIC
homozygous
137998267
7
8190202
8190203
G
C
30
GENIC
homozygous
137998268
7
8190564
8190565
G
T
23
GENIC
homozygous
137998269
7
8190600
8190601
T
C
25
GENIC
homozygous
137998270
7
8190644
8190645
G
A
20
GENIC
homozygous
137998271
7
8190645
8190646
C
A
20
GENIC
homozygous
137998272
7
8190726
8190727
C
A
23
GENIC
homozygous
137998273
7
8191391
8191392
A
G
19
GENIC
homozygous
137998274
7
8191427
8191428
G
A
20
GENIC
homozygous
137998275
7
8191587
8191588
G
T
17
GENIC
homozygous
137998276
7
8191679
8191680
A
G
25
GENIC
homozygous
137998277
7
8192675
8192675
C
20
GENIC
homozygous
137934269
7
8199542
8199543
C
T
21
GENIC
homozygous
137998278
7
8200834
8200834
CTGTGGG
22
GENIC
homozygous
137934270
7
8202010
8202010
GGTGGGCTTCACATCTAGAGTACAGAT
27
GENIC
homozygous
137934271
7
8202323
8202324
T
G
19
GENIC
homozygous
137998279
7
8202626
8202626
TTCTTTT
19
GENIC
homozygous
137934272
7
8202677
8202678
G
A
11
GENIC
homozygous
137998280
7
8202988
8202989
T
G
15
GENIC
homozygous
137998281
7
8204617
8204618
A
G
18
GENIC
homozygous
137998282
7
8205305
8205306
T
A
30
GENIC
possibly homozygous
137998283
7
8205464
8205465
G
A
23
GENIC
homozygous
137998284
7
8187321
8187322
A
10
GENIC
heterozygous
403199273
7
8187321
8187322
A
G
10
GENIC
homozygous
154420504
7
8193821
8193822
A
15
GENIC
heterozygous
146816991
7
8193821
8193822
A
G
15
GENIC
homozygous
154420507
