chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108993039589930396GC15GENIChomozygous116982567
108993068689930687TC15GENIChomozygous116903703
108993069189930692CT15GENIChomozygous116950838
108993139889931399GA5GENIChomozygous116950840
108993205889932059CT10GENIChomozygous116950842
108993319589933196AT17GENIChomozygous116950844
108993330989933310CT14GENIChomozygous116982569
108993423989934240TC18GENIChomozygous116950850
108993515289935153CT16GENIChomozygous116950856
108993557489935575GA21GENIChomozygous116950858
108993636689936367CT20GENIChomozygous116950860
108993693789936938AT16GENIChomozygous116950862
108993713089937131CA19GENIChomozygous116950864
108993725189937252CT17GENIChomozygous116950866
108993727689937277CT19GENIChomozygous116950868
108993728289937283CT18GENIChomozygous116950870
108993728889937289GT17GENIChomozygous116950872
108993730889937309TC15GENIChomozygous116950874
108993746289937463CT20GENIChomozygous116950876
108993809689938097TC22GENIChomozygous116950878
108993829789938298CT14GENIChomozygous116950880
108994005289940053AG21GENIChomozygous116950882
108994760489947605TG17GENIChomozygous116950884
108995036389950364AG4GENIChomozygous116950886
108995210189952102AG21GENIChomozygous116903713
108995286489952865CT25GENIChomozygous117087835
108995304589953046AG11GENIChomozygous116903717
108995373689953737TC12GENIChomozygous116903721
108995507489955075TC14GENIChomozygous116903723
108995507689955077GA16GENIChomozygous116950888
108995508789955088TC16GENIChomozygous116982571
108995778989957790CT12GENIChomozygous116950890
108995906189959062CT3GENIChomozygous116950892