chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108637551986375520AT9GENIChomozygous138842256
108637586386375864TC22GENIChomozygous138842258
108637598786375988GA24GENIChomozygous143463658
108637630686376307AC20GENIChomozygous143463659
108637643786376438AC20GENIChomozygous143463660
108637704886377049TG11GENIChomozygous143463661
108637753286377533GA18GENIChomozygous138842260
108637760786377608GA15GENIChomozygous143463662
108637773686377737AG15GENIChomozygous143463663
108637778586377786GT14GENIChomozygous143463664
108637788986377890CT19GENIChomozygous143463665
108637792586377926GA16GENIChomozygous143463666
108637798186377982AG18GENIChomozygous143463667
108637862786378628CT14GENIChomozygous143463668
108637873186378732CG15GENIChomozygous138842264
108637877586378776GA18GENIChomozygous143463669
108637725186377252G15GENICheterozygous403293771
108637712186377122CT9GENICheterozygous154660060
108637717686377177TC16GENICpossibly homozygous154660062
108637725186377252GA15GENICpossibly homozygous154660063
108637827986378279T15GENIChomozygous138697007
108637815486378154AC17GENIChomozygous143435106
108637908286379083T24GENIChomozygous143435107
108637707286377081AAGTGTAGA8GENICheterozygous144077615
108637712186377122C9GENICheterozygous403293769
108637717686377177T16GENICheterozygous403293770