chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4210999273210999274GC38GENIChomozygous510253693
4210999289210999296ACCAGGC-------19GENIChomozygous685581016
4210999699210999700TC57GENIChomozygous506635933
4210999739210999740TC69GENIChomozygous506635934
4211000292211000293TA58GENIChomozygous506635935
4211000306211000307AG57GENIChomozygous506635936
4211000436211000438GT--43GENIChomozygous685581017
4211000448211000449CA45GENIChomozygous510253694
4211001064211001065TC70GENIChomozygous506635937
4211001945211001946CT59GENICpossibly homozygous510253695
4211002129211002130AT45GENIChomozygous506635938
4211002190211002191GA40GENIChomozygous506635939
4211002241211002242TTCGAA38GENIChomozygous685581018
4211002372211002373CCCATGGGCCG19GENIChomozygous685581019