chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
11
41883565
41883566
T
C
19
GENIC
possibly homozygous
154696286
11
41883573
41883573
G
18
GENIC
possibly homozygous
138886116
11
41884599
41884600
T
C
60
GENIC
homozygous
138979833
11
41884548
41884549
C
T
63
GENIC
homozygous
138979830
11
41884561
41884562
C
G
65
GENIC
homozygous
138979831
11
41884568
41884569
A
G
65
GENIC
homozygous
138979832
11
41884781
41884782
A
G
65
GENIC
homozygous
138979834
11
41886768
41886769
C
T
52
GENIC
homozygous
138979835
11
41886777
41886778
C
51
GENIC
homozygous
138886117
11
41887389
41887392
AAG
49
GENIC
possibly homozygous
138886118
11
41887391
41887392
G
A
49
GENIC
heterozygous
154696288
11
41887391
41887392
G
49
GENIC
possibly homozygous
403304770
11
41887531
41887531
GATGTTCTTAAGGGAAGGAAGCGGTGCACA
45
GENIC
homozygous
138886119
11
41889330
41889331
A
C
37
GENIC
homozygous
138979836
