chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1206276726206276727GC31GENICpossibly homozygous61318388
1206276750206276751GA37GENICpossibly homozygous61066528
1206279112206279113GA37GENIChomozygous61066532
1206279581206279591TTTTGTTTTG----------14GENIChomozygous61066533
1206284363206284364GA51GENIChomozygous61066534
1206289468206289469GGGT11GENICheterozygous61066537
1206289788206289789C-46GENIChomozygous61066539
1206289979206289980AAT52GENIChomozygous61066540
1206290063206290068ACACA-----43GENIChomozygous61066541
1206290065206290068ACA---43GENIChomozygous61066542
1206290067206290070AAA---42GENICheterozygous61066543
1206290067206290068AAC43GENIChomozygous61066544
1206290069206290070A-42GENICpossibly homozygous61066545
1206291901206291902TC38GENIChomozygous62030874
1206292265206292266GGAC10GENICheterozygous61066548
1206292298206292299GA22GENICpossibly homozygous61066549
1206292303206292305CA--17GENICheterozygous62030875