chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144473794144473796AT31GENIChomozygous137347694
5144474329144474330G17GENIChomozygous137347695
5144474329144474330GT17GENICheterozygous403161875
5144474424144474424CTTC24GENIChomozygous137347696
5144475558144475558A35GENIChomozygous137347697
5144478152144478153TG12GENICheterozygous154255806
5144478152144478153T12GENICheterozygous403161876
5144478160144478161TG12GENICheterozygous137645759
5144475484144475485TC19GENIChomozygous137645756
5144475498144475499CT24GENIChomozygous137645757
5144476337144476338GT35GENIChomozygous137645758
5144479129144479130CT46GENIChomozygous137645760
5144482456144482457T6GENICheterozygous403161877
5144482456144482457TC6GENICheterozygous403161878
5144482458144482459T6GENICheterozygous403161879
5144482458144482459TC6GENICheterozygous403161880
5144482458144482459TG6GENICheterozygous403161881
5144482460144482461T6GENICheterozygous403161882
5144482460144482461TC6GENICheterozygous403161883
5144482462144482463T6GENICheterozygous403161884
5144482462144482463TC6GENICheterozygous403161885
5144482669144482670AG16GENIChomozygous137645761
5144478162144478163TG12GENICheterozygous145548793
5144482847144482847TC24GENIChomozygous137347698
5144483059144483060GA41GENIChomozygous137645762
5144484385144484386CA25GENIChomozygous137645763
5144485234144485235TC6GENIChomozygous137645764
5144485288144485289AG12GENIChomozygous137645765
5144485475144485476CG19GENIChomozygous137645766
5144486868144486869TC44GENIChomozygous137645767