chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
149977524499775245TC26GENIChomozygous113517520
149977526999775270CA27GENIChomozygous113517522
149977594999775950AG27GENIChomozygous113517524
149977631799776318CT9GENIChomozygous113517526
149977639799776398TC11GENIChomozygous113517528
149977661799776618GA15GENIChomozygous113517530
149977665299776653TC13GENIChomozygous113517532
149977665499776655GC13GENIChomozygous113517534
149977692099776921AG15GENIChomozygous113517536
149977703799777038GA23GENIChomozygous113517538
149977744099777441AG35GENIChomozygous113517548
149977709299777093CT15GENIChomozygous113517540
149977711199777112CA25GENIChomozygous113517542
149977730199777302GA20GENIChomozygous113517544
149977730699777307GA20GENIChomozygous113517546
149977772199777722AG21GENIChomozygous113517550
149977832499778325TG19GENIChomozygous113517552
149977910699779107AG22GENIChomozygous113517554
149977932999779330GA33GENIChomozygous113517556
149977990299779903TC23GENIChomozygous113517558
149977998799779988AG22GENIChomozygous113517560
149978001499780015TC19GENIChomozygous113517562
149978039599780396AG11GENIChomozygous113517564
149978043199780432GC9GENIChomozygous113517566
149978043599780436CG9GENIChomozygous113517568
149978058199780582GC12GENIChomozygous113517570