chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
149977524499775245TC18GENIChomozygous113517520
149977526999775270CA22GENIChomozygous113517522
149977594999775950AG17GENIChomozygous113517524
149977631799776318CT17GENIChomozygous113517526
149977639799776398TC23GENIChomozygous113517528
149977661799776618GA26GENIChomozygous113517530
149977665299776653TC27GENIChomozygous113517532
149977665499776655GC27GENIChomozygous113517534
149977692099776921AG28GENIChomozygous113517536
149977703799777038GA24GENIChomozygous113517538
149977709299777093CT27GENIChomozygous113517540
149977711199777112CA31GENIChomozygous113517542
149977730199777302GA26GENIChomozygous113517544
149977730699777307GA27GENIChomozygous113517546
149977744099777441AG23GENIChomozygous113517548
149977772199777722AG22GENIChomozygous113517550
149977832499778325TG30GENIChomozygous113517552
149977910699779107AG40GENIChomozygous113517554
149977932999779330GA35GENIChomozygous113517556
149977990299779903TC22GENIChomozygous113517558
149977998799779988AG16GENIChomozygous113517560
149978001499780015TC15GENIChomozygous113517562
149978039599780396AG23GENIChomozygous113517564
149978043199780432GC18GENIChomozygous113517566
149978043599780436CG17GENIChomozygous113517568
149978058199780582GC13GENIChomozygous113517570