chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4210999273210999274GC28GENICpossibly homozygous655985687
4210999289210999296ACCAGGC-------27GENICpossibly homozygous760614179
4210999699210999700TC25GENIChomozygous655985688
4210999739210999740TC26GENIChomozygous655985689
4211000292211000293TA26GENIChomozygous655985690
4211000306211000307AG27GENIChomozygous655985691
4211000436211000438GT--31GENIChomozygous760614180
4211001064211001065TC26GENIChomozygous655985692
4211001945211001946CT29GENIChomozygous655985693
4211002129211002130AT39GENIChomozygous655985694
4211002190211002191GA35GENIChomozygous655985695
4211002241211002242TTCGAA44GENIChomozygous760614181
4211002372211002373CCCATGGGCCG35GENIChomozygous760614182