chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
13
50090378
50090380
GT
--
43
GENIC
heterozygous
49755362
13
50090492
50090494
GT
--
47
GENIC
heterozygous
50601901
13
50097348
50097349
G
GTGTGTGTGTATGTGTGTGTGCATGTTTGTGTGTCTGTGTGTATGTTTGTGTATGTGTATGTGTGAGTGTGTGAGTGTGTGTGTGTGTGCATGTTTGTGTGTCTGTGTGTATGTTTGTGTATGTGTGTGTATGTGTGCATTTTTGTGGGTCTGTGTGTATGTTTGTGTATGTGTGAGTGTGTGTGTATGTGTGTGTGCATGTTTGTGTGTCTGTGTGTATGTTTGTGTA
36
GENIC
possibly homozygous
50517579
13
50106753
50106754
G
GT
42
GENIC
homozygous
49755372
13
50106773
50106828
CCCCCCCCCCAGGGAACTTCCCCCTTTGGGGGTGTAACCATTCCCCAGGGCAGGC
-------------------------------------------------------
44
GENIC
homozygous
50517580
13
50106837
50106838
C
G
14
GENIC
homozygous
49755378
13
50106840
50106841
C
A
18
GENIC
homozygous
49755379
13
50106850
50106851
G
-
16
GENIC
homozygous
49755380
13
50106856
50106857
C
-
19
GENIC
homozygous
49755381
13
50106862
50106863
C
-
16
GENIC
homozygous
49755382
13
50106870
50106871
T
-
17
GENIC
homozygous
49755383
13
50106875
50106876
C
A
22
GENIC
homozygous
50517581
13
50106876
50106877
G
C
24
GENIC
homozygous
50517582
13
50106883
50106884
A
T
32
GENIC
homozygous
49755384
13
50106896
50106897
G
-
39
GENIC
homozygous
49755385
13
50106907
50106908
G
T
43
GENIC
homozygous
49755386
13
50106909
50106910
A
-
44
GENIC
homozygous
49755387
