chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4210999273210999274GC33GENIChomozygous505550146
4210999289210999296ACCAGGC-------19GENIChomozygous683862484
4210999699210999700TC42GENICpossibly homozygous501997006
4210999739210999740TC49GENIChomozygous501997007
4211000292211000293TA43GENIChomozygous501997008
4211000306211000307AG42GENIChomozygous501997009
4211000436211000438GT--51GENIChomozygous683862485
4211000448211000449CA59GENIChomozygous505550147
4211001064211001065TC51GENIChomozygous501997010
4211001945211001946CT64GENICpossibly homozygous505550148
4211002129211002130AT41GENIChomozygous501997011
4211002190211002191GA35GENIChomozygous501997012
4211002241211002242TTCGAA21GENIChomozygous683862486
4211002244211002245GA25GENICheterozygous505550149
4211002372211002373CCCATGGGCCG5GENIChomozygous683862487