chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
83638224236382243TC34GENIChomozygous116456461
83638240636382407TC40GENIChomozygous116456462
83638246936382470TC42GENIChomozygous116456463
83638257336382574GA32GENIChomozygous116456464
83638257936382580GA29GENIChomozygous116456465
83638258136382582TC28GENIChomozygous116456466
83638259636382597CT30GENIChomozygous116456467
83638261336382614CT34GENIChomozygous116456468
83638261536382616GA34GENIChomozygous116456469
83638321736383218GC19GENIChomozygous116456470
83638348036383481CT12GENIChomozygous116456471
83638406836384069GA22GENICheterozygous116456473
83638441136384412TC31GENIChomozygous116456474
83638598036385981TA35GENIChomozygous116456475
83638617836386179AC44GENIChomozygous116456476
83638658436386585TC49GENIChomozygous116456477
83638661636386617TC47GENIChomozygous116456478
83638684736386848TC19GENIChomozygous116456479
83638708736387088CT7GENIChomozygous116456480
83638719236387193GA9GENIChomozygous116456481
83638736336387364TG26GENIChomozygous116456482
83638933136389332GA29GENIChomozygous116456483
83638987136389872GC23GENIChomozygous116456484
83639104936391050GT16GENIChomozygous116456485
83639219736392198GT11GENIChomozygous116456486
83639236736392368CT26GENIChomozygous116456487
83639299036392991AG18GENIChomozygous116456488
83639305536393056AG18GENIChomozygous116456489
83639321536393216TC21GENIChomozygous116456490
83639345536393456TC11GENICpossibly homozygous116456491
83639346336393464TC11GENICpossibly homozygous116456492
83639346936393470AT16GENICheterozygous116456493
83639484336394844GA16GENIChomozygous116456494
83639559736395598GA30GENIChomozygous116456495
83639559836395599CT29GENIChomozygous116456496
83639574936395750AG24GENIChomozygous116456497
83639917136399172GA21GENIChomozygous116456498
83639956236399563TC16GENIChomozygous116456499