chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5160328202160328203GA13GENIChomozygous114074083
5160329735160329736CT21GENIChomozygous114074084
5160332931160332932CG18GENIChomozygous114074085
5160333141160333142TC22GENIChomozygous114074086
5160333684160333685CG12GENIChomozygous114074087
5160334201160334202AC18GENIChomozygous114074088
5160335239160335240AT11GENIChomozygous114074089
5160335433160335434GC15GENIChomozygous114074090
5160336588160336589GA16GENIChomozygous114074091
5160337021160337022GA11GENIChomozygous114074092
5160337537160337538CA27GENIChomozygous114074093
5160338308160338309AC15GENIChomozygous114074094
5160338349160338350TA19GENIChomozygous114074095
5160340524160340525CA19GENIChomozygous114074096
5160342087160342088AG22GENIChomozygous114074097
5160342408160342409AG18GENIChomozygous114074098
5160342576160342577CA21GENIChomozygous114074099
5160342711160342712CT15GENIChomozygous114074100
5160344291160344292GA22GENIChomozygous114074101
5160345160160345161AC19GENIChomozygous114074102
5160345424160345425CT26GENIChomozygous114074103
5160345676160345677AG6GENIChomozygous114074104
5160346657160346658AG17GENIChomozygous114074106
5160346739160346740TC20GENIChomozygous114074107
5160350090160350091AG25GENIChomozygous114074108
5160350280160350281GA17GENIChomozygous114074109