chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1172877062172877063CG19GENICpossibly homozygous108386400
1172877125172877126TA24GENICpossibly homozygous108386402
1172877209172877210CT22GENIChomozygous108386404
1172877237172877238TC20GENIChomozygous120474725
1172877238172877239CT20GENIChomozygous120474726
1172877342172877343CT16GENICpossibly homozygous108386406
1172877434172877435TC23GENIChomozygous108386408
1172877513172877514GA18GENIChomozygous108386410
1172877539172877540CT20GENIChomozygous108386412
1172877660172877661GA18GENICpossibly homozygous108386414