chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
12
39931424
39931425
G
A
29
GENIC
homozygous
50202164
12
39932363
39932364
A
AGCATGGGGAG
3
GENIC
homozygous
50512176
12
39932996
39932997
G
A
16
GENIC
homozygous
50202201
12
39933120
39933121
T
TA
10
GENIC
possibly homozygous
50202203
12
39937265
39937266
G
A
20
GENIC
homozygous
50202223
12
39940259
39940260
G
A
17
GENIC
possibly homozygous
50202232
12
39942413
39942414
G
A
9
GENIC
homozygous
50202236
12
39944702
39944703
T
C
10
GENIC
homozygous
50202238
12
39947121
39947122
G
-
9
GENIC
homozygous
50202244
12
39947606
39947607
T
G
20
GENIC
possibly homozygous
50202246
12
39948719
39948720
A
G
20
GENIC
homozygous
50202248
12
39949426
39949427
A
-
1
GENIC
homozygous
50202249
12
39952655
39952656
T
A
23
GENIC
possibly homozygous
50202253
12
39953224
39953271
GCTGCACTTACACTGCTGTTGGTCATTACACAGCATGCCTCGGCAAC
-----------------------------------------------
17
GENIC
homozygous
50512178
12
39953357
39953358
T
C
2
GENIC
homozygous
50202261
12
39954012
39954013
A
-
4
GENIC
homozygous
50202265
12
39954275
39954276
A
G
7
GENIC
homozygous
50202267
12
39954283
39954284
G
A
9
GENIC
homozygous
50202269
12
39954840
39954841
C
G
15
GENIC
homozygous
50202275
12
39954970
39954971
C
A
18
GENIC
possibly homozygous
50202277
12
39955001
39955002
G
A
21
GENIC
possibly homozygous
50202279
12
39955889
39955890
A
G
34
GENIC
possibly homozygous
50202281
12
39956087
39956088
C
CAGGG
3
GENIC
homozygous
50512180
12
39956789
39956790
G
A
9
GENIC
heterozygous
50202293
12
39958244
39958245
C
T
13
GENIC
heterozygous
50202299
12
39963557
39963558
A
AG
2
GENIC
heterozygous
50512182
12
39963951
39963952
G
A
18
GENIC
possibly homozygous
50202301
