chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142410380024103801TG17GENIChomozygous942107353
142410385924103860TA14GENIChomozygous942107354
142410427124104272TC21GENIChomozygous942107355
142410436724104368TC16GENIChomozygous942107356
142410441624104417GC21GENIChomozygous942107357
142410456424104565GA16GENIChomozygous942107358
142410471824104719GA16GENIChomozygous942107359
142410474224104743TC11GENIChomozygous942107360
142410961424109615TC17GENIChomozygous942107361
142410964224109643CT19GENIChomozygous942107362
142410982324109824GT8GENIChomozygous942107363
142410989424109895GT11GENIChomozygous942107364
142410999024109991GC17GENIChomozygous942107365
142411653724116538TC14GENIChomozygous942107366
142411671024116711GA9GENIChomozygous942107367
142411704524117046AC22GENIChomozygous942107368
142411943824119439TA17GENIChomozygous942107369
142411988824119889GA28GENIChomozygous942107370
142412123724121238GA9GENIChomozygous942107371
142412148724121488GA12GENIChomozygous942107372
142412186924121870AT28GENIChomozygous942107373
142412329224123293GT24GENIChomozygous942107374
142412331324123314GC23GENIChomozygous942107375
142412389124123892GC18GENIChomozygous942107376
142412462824124629AG6GENIChomozygous942107377
142412524224125243TC23GENIChomozygous942107378