chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142410380024103801TG11GENIChomozygous950809417
142410385924103860TA17GENIChomozygous950809418
142410427124104272TC19GENIChomozygous950809419
142410436724104368TC23GENIChomozygous950809420
142410441624104417GC22GENIChomozygous950809421
142410456424104565GA25GENIChomozygous950809422
142410471824104719GA18GENIChomozygous950809423
142410474224104743TC22GENIChomozygous950809424
142410961424109615TC23GENIChomozygous950809425
142410964224109643CT25GENIChomozygous950809426
142410982324109824GT15GENIChomozygous950809427
142410989424109895GT17GENIChomozygous950809428
142410999024109991GC10GENIChomozygous950809429
142411653724116538TC26GENIChomozygous950809430
142411671024116711GA25GENIChomozygous950809431
142411704524117046AC17GENIChomozygous950809432
142411943824119439TA19GENIChomozygous950809433
142411988824119889GA24GENIChomozygous950809434
142412123724121238GA26GENIChomozygous950809435
142412148724121488GA28GENIChomozygous950809436
142412186924121870AT34GENIChomozygous950809437
142412329224123293GT19GENIChomozygous950809438
142412331324123314GC25GENIChomozygous950809439
142412389124123892GC22GENIChomozygous950809440
142412462824124629AG14GENIChomozygous950809441
142412524224125243TC23GENIChomozygous950809442