chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3124517770124517771GC50GENIChomozygous111694446
3124519228124519229AG4GENIChomozygous112297989
3124519302124519303TC9GENIChomozygous111694447
3124519306124519307AC10GENIChomozygous111694448
3124519964124519965CA46GENIChomozygous111694449
3124521401124521402TC35GENIChomozygous111694450
3124521522124521523TC59GENIChomozygous111694451
3124521741124521742CT46GENIChomozygous111694452
3124522300124522301AG34GENIChomozygous111694453
3124522628124522629CT15GENIChomozygous111694454
3124522785124522786TC41GENIChomozygous111694455
3124523340124523341AT46GENIChomozygous111694456
3124523651124523652AG40GENIChomozygous111694457
3124523795124523796CT21GENIChomozygous111694458
3124524132124524133CA49GENIChomozygous111694459
3124525019124525020AG29GENIChomozygous111694460
3124525044124525045CT29GENIChomozygous111694461
3124525225124525226GA44GENIChomozygous111694462
3124526061124526062TC46GENIChomozygous111694463
3124526128124526129AC35GENIChomozygous111694464
3124526148124526149GA35GENIChomozygous111694465
3124526190124526191CT30GENIChomozygous111694466
3124528436124528437TC34GENIChomozygous111694467
3124530504124530505AT45GENIChomozygous111694468
3124531088124531089GA33GENIChomozygous111694469