chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221540008221540009TC42GENIChomozygous108995032
1221540877221540878GA38GENIChomozygous108995033
1221541550221541551AG46GENIChomozygous108995034
1221541596221541597GA37GENIChomozygous108995035
1221541726221541727CT44GENICpossibly homozygous108995036
1221542473221542474GA44GENIChomozygous108995037
1221542951221542952TC59GENIChomozygous108544607
1221543843221543844TC53GENIChomozygous108544613
1221544142221544143GA55GENIChomozygous108995038
1221544691221544692TG61GENIChomozygous108544615
1221545705221545706GC40GENIChomozygous108544619
1221546317221546318CT27GENICpossibly homozygous108995039
1221546390221546391CT19GENIChomozygous108995040