chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4210999273210999274GC29GENICpossibly homozygous644580360
4210999289210999296ACCAGGC-------27GENIChomozygous753818421
4210999699210999700TC26GENICpossibly homozygous644580361
4210999739210999740TC26GENIChomozygous644580362
4211000292211000293TA28GENIChomozygous644580363
4211000306211000307AG26GENIChomozygous644580364
4211000436211000438GT--34GENIChomozygous753818422
4211001064211001065TC27GENIChomozygous644580365
4211001945211001946CT29GENIChomozygous644580366
4211002129211002130AT32GENIChomozygous644580367
4211002190211002191GA26GENIChomozygous644580368
4211002241211002242TTCGAA25GENIChomozygous753818423
4211002372211002373CCCATGGGCCG32GENIChomozygous753818424