chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101400583314005834AG15GENIChomozygous51622556
101400790314007904CT16GENIChomozygous51622557
101400819914008200AG11GENIChomozygous51622558
101400844314008444AC23GENIChomozygous51622559
101400863114008632TC16GENIChomozygous51622560
101400880714008808GA23GENIChomozygous51622561
101401070814010709GGACAC11GENICheterozygous51622562
101401070814010709GGACACAC11GENICheterozygous51622563
101401070814010709GGACACACAC11GENICheterozygous51809986
101401261114012612CT9GENIChomozygous51622564
101401296514012966AG19GENIChomozygous51622565
101401356114013562G-13GENIChomozygous51622566
101401356414013568TTTG----13GENIChomozygous51622568
101401386514013866TC14GENIChomozygous51622569
101401394514013946TC13GENIChomozygous51622570
101401413914014140AAT11GENIChomozygous51622571
101401422014014221AT1GENIChomozygous51622572
101401480114014802TTA23GENIChomozygous51622574
101401480214014803TA25GENIChomozygous51622575
101401490714014908GA11GENIChomozygous51622576
101401423614014237AATTTTT2GENIChomozygous52481268
101401247414012527TGTGTGCCACCCCCACCCTGTGTGCCACCCCCACCCTGTGTGCCACCCCACCG-----------------------------------------------------7GENICheterozygous52313037