chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
44952739649527397TC6GENIChomozygous56876402
44952745849527459TC16GENIChomozygous56876405
44952751149527512TC12GENIChomozygous56876408
44952767149527672TG1GENIChomozygous56876411
44952770949527710T-9GENIChomozygous56876414
44952779849527799TC14GENICpossibly homozygous56876417
44952824049528241CT16GENIChomozygous56876420
44952863949528640CT13GENICheterozygous56876426
44952874849528749CT19GENICpossibly homozygous56876429
44952879049528791CT16GENICpossibly homozygous56876431
44952948249529483GA12GENIChomozygous56876434
44952949949529500CT11GENIChomozygous56876437
44952970349529704TC15GENIChomozygous56876440
44953039949530400CCTT1GENIChomozygous56876443
44953071549530716AG12GENICheterozygous56876458
44953082349530824GGAA2GENIChomozygous56876461