chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101400583314005834AG7GENIChomozygous51622556
101400790314007904CT13GENIChomozygous51622557
101400819914008200AG21GENIChomozygous51622558
101400844314008444AC18GENIChomozygous51622559
101400863114008632TC21GENIChomozygous51622560
101400880714008808GA20GENIChomozygous51622561
101401070814010709GGACAC18GENICheterozygous51622562
101401070814010709GGACACAC18GENICheterozygous51622563
101401247414012527TGTGTGCCACCCCCACCCTGTGTGCCACCCCCACCCTGTGTGCCACCCCACCG-----------------------------------------------------10GENICheterozygous52313037
101401261114012612CT20GENIChomozygous51622564
101401296514012966AG20GENIChomozygous51622565
101401356114013562G-26GENIChomozygous51622566
101401356414013568TTTG----26GENIChomozygous51622568
101401386514013866TC19GENIChomozygous51622569
101401394514013946TC13GENIChomozygous51622570
101401413914014140AAT1GENIChomozygous51622571
101401422014014221AT3GENIChomozygous51622572
101401480114014802TTA15GENIChomozygous51622574
101401480214014803TA15GENIChomozygous51622575
101401490714014908GA27GENIChomozygous51622576
101401423614014237AATTTTT4GENIChomozygous52481268