chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5173591718173591719CT25GENIChomozygous114094923
5173591722173591723CG27GENIChomozygous114094924
5173591802173591803CA25GENICpossibly homozygous114094925
5173593153173593154TG30GENICpossibly homozygous114094931
5173593159173593160CT31GENICpossibly homozygous114094932
5173593909173593910GA26GENIChomozygous114094933
5173594601173594602TC10GENIChomozygous114094934
5173598231173598232AG13GENIChomozygous114094935
5173599842173599843TC35GENIChomozygous114094936
5173602640173602641AG19GENIChomozygous114094938
5173604724173604725GA16GENIChomozygous114094939
5173606005173606006CT15GENIChomozygous114094940
5173606400173606401CT27GENIChomozygous114094941
5173607235173607236TC12GENIChomozygous114094942
5173607979173607980TC26GENIChomozygous114094945
5173608144173608145GA20GENIChomozygous114094946
5173612050173612051CT18GENIChomozygous114094947
5173614062173614063GA34GENIChomozygous114094948
5173614141173614142CT20GENIChomozygous114094949
5173615685173615686TC31GENIChomozygous114094951
5173615755173615756GA20GENIChomozygous114094952
5173620242173620243CT28GENICpossibly homozygous114094953
5173620288173620289TC19GENIChomozygous114094954
5173622507173622508AC8GENIChomozygous114094955