chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
12
14782427
14782428
C
CGCCCT
5
GENIC
homozygous
50434583
12
14782588
14782589
A
AACACACACACACACACACACACACACACAC
3
GENIC
homozygous
50533266
12
14783696
14783697
T
TCTCTCTCACACACACA
16
GENIC
homozygous
50533270
12
14784148
14784149
G
GT
19
GENIC
homozygous
50434585
12
14784151
14784152
G
GT
21
GENIC
possibly homozygous
50069363
12
14785166
14785167
T
C
37
GENIC
homozygous
50069365
12
14785176
14785177
T
C
37
GENIC
homozygous
50069367
12
14785400
14785401
A
G
33
GENIC
homozygous
50069369
12
14786582
14786583
T
C
41
GENIC
homozygous
50069375
12
14786794
14786795
G
C
20
GENIC
homozygous
50069379
12
14787810
14787811
C
T
24
GENIC
homozygous
50069381
12
14788159
14788160
A
G
1
GENIC
homozygous
50533276
12
14788163
14788164
A
G
1
GENIC
homozygous
50533278
12
14788201
14788202
G
A
8
GENIC
heterozygous
50533280
12
14788215
14788219
GAGC
----
6
GENIC
homozygous
50503971
12
14788277
14788278
C
A
17
GENIC
homozygous
50434587
12
14788746
14788747
G
T
30
GENIC
homozygous
50434589
12
14788891
14788892
C
T
35
GENIC
homozygous
50434591
12
14789181
14789190
TTTTTTTTG
---------
20
GENIC
possibly homozygous
50069389
12
14789726
14789727
C
A
36
GENIC
homozygous
50434593
12
14790627
14790628
C
CA
36
GENIC
homozygous
50434595
