chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6114475221114475222GA17GENIChomozygous115473470
6114475251114475252GA22GENIChomozygous114949793
6114475389114475390AG43GENIChomozygous114949795
6114476426114476427AG22GENIChomozygous114949799
6114476505114476506AG24GENIChomozygous114949801
6114477083114477084CA33GENIChomozygous114949803
6114479882114479883AG27GENIChomozygous114949807
6114479906114479907AG32GENIChomozygous114949808
6114480548114480549TA32GENIChomozygous115473472
6114480780114480781CG36GENIChomozygous114949810
6114481638114481639CT23GENIChomozygous115473474
6114481940114481941CT24GENIChomozygous115473476
6114482354114482355TC24GENIChomozygous114949814
6114482877114482878AG27GENIChomozygous115473478
6114483464114483465GA25GENIChomozygous115473480
6114483832114483833GA35GENICpossibly homozygous115473482
6114483870114483871AG27GENIChomozygous114949818
6114488152114488153CT82GENICheterozygous115473484