chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
12
49197335
49197336
T
TTGG
7
GENIC
homozygous
50546645
12
49197336
49197337
C
G
7
GENIC
homozygous
50546646
12
49197339
49197340
A
T
6
GENIC
homozygous
50546647
12
49197347
49197348
A
AGCTCAGTGGTAGAGCGCTTGCCTAGC
5
GENIC
homozygous
50546648
12
49197349
49197350
A
AGC
5
GENIC
homozygous
50546649
12
49205244
49205245
C
-
9
GENIC
heterozygous
50655436
12
49207361
49207362
C
CT
19
GENIC
possibly homozygous
50491969
12
49211776
49211777
T
G
10
GENIC
heterozygous
50231963
12
49212776
49212777
G
-
21
GENIC
homozygous
50231971
12
49220533
49220579
TTTATAGCGAATCAGGCACACCTGGCTGTTTGTTGCCAGGTAACTG
----------------------------------------------
9
GENIC
homozygous
50546652