chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4210999273210999274GC29GENIChomozygous663263597
4210999289210999296ACCAGGC-------26GENIChomozygous765048269
4210999699210999700TC28GENIChomozygous663263598
4210999739210999740TC32GENIChomozygous663263599
4211000292211000293TA30GENIChomozygous663263600
4211000306211000307AG35GENIChomozygous663263601
4211000436211000438GT--37GENIChomozygous765048270
4211001064211001065TC26GENIChomozygous663263602
4211001945211001946CT31GENICpossibly homozygous663263603
4211002129211002130AT29GENIChomozygous663263604
4211002190211002191GA27GENIChomozygous663263605
4211002241211002242TTCGAA29GENIChomozygous765048271
4211002372211002373CCCATGGGCCG23GENIChomozygous765048272