chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4210999273210999274GC33GENIChomozygous634106521
4210999289210999296ACCAGGC-------26GENIChomozygous747230734
4210999699210999700TC21GENIChomozygous634106522
4210999739210999740TC17GENIChomozygous634106523
4211000292211000293TA23GENIChomozygous634106524
4211000306211000307AG24GENIChomozygous634106525
4211000436211000438GT--18GENIChomozygous747230735
4211001064211001065TC25GENIChomozygous634106526
4211001945211001946CT34GENICpossibly homozygous634106527
4211002129211002130AT37GENIChomozygous634106528
4211002190211002191GA26GENIChomozygous634106529
4211002241211002242TTCGAA24GENIChomozygous747230736
4211002372211002373CCCATGGGCCG9GENIChomozygous747230737