chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101400583314005834AG16GENIChomozygous51622556
101400790314007904CT30GENIChomozygous51622557
101400819914008200AG25GENIChomozygous51622558
101400844314008444AC23GENIChomozygous51622559
101400863114008632TC21GENIChomozygous51622560
101400880714008808GA22GENIChomozygous51622561
101401070814010709GGACAC13GENICheterozygous51622562
101401070814010709GGACACAC13GENICheterozygous51622563
101401247414012527TGTGTGCCACCCCCACCCTGTGTGCCACCCCCACCCTGTGTGCCACCCCACCG-----------------------------------------------------14GENICheterozygous52313037
101401261114012612CT17GENIChomozygous51622564
101401296514012966AG28GENIChomozygous51622565
101401356114013562G-22GENIChomozygous51622566
101401356414013568TTTG----22GENIChomozygous51622568
101401386514013866TC18GENIChomozygous51622569
101401394514013946TC7GENIChomozygous51622570
101401413914014140AAT13GENIChomozygous51622571
101401422014014221AT8GENIChomozygous51622572
101401480114014802TTA17GENIChomozygous51622574
101401480214014803TA18GENIChomozygous51622575
101401490714014908GA17GENIChomozygous51622576
101401423614014237AATTTTT11GENIChomozygous52481268