chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
149977524499775245TC24GENIChomozygous113517520
149977526999775270CA24GENIChomozygous113517522
149977594999775950AG29GENIChomozygous113517524
149977631799776318CT13GENIChomozygous113517526
149977639799776398TC19GENIChomozygous113517528
149977661799776618GA38GENIChomozygous113517530
149977665299776653TC33GENIChomozygous113517532
149977665499776655GC33GENIChomozygous113517534
149977692099776921AG36GENIChomozygous113517536
149977703799777038GA20GENIChomozygous113517538
149977709299777093CT21GENIChomozygous113517540
149977711199777112CA26GENIChomozygous113517542
149977730199777302GA30GENIChomozygous113517544
149977730699777307GA29GENIChomozygous113517546
149977744099777441AG34GENIChomozygous113517548
149977772199777722AG29GENIChomozygous113517550
149977832499778325TG28GENIChomozygous113517552
149977910699779107AG27GENIChomozygous113517554
149977932999779330GA28GENIChomozygous113517556
149977990299779903TC24GENIChomozygous113517558
149977998799779988AG28GENIChomozygous113517560
149978001499780015TC28GENIChomozygous113517562
149978039599780396AG20GENIChomozygous113517564
149978043199780432GC24GENIChomozygous113517566
149978043599780436CG23GENIChomozygous113517568
149978058199780582GC15GENIChomozygous113517570