chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1258210342258210343CT16GENIChomozygous108781807
1258210979258210980TC12GENIChomozygous108624222
1258211432258211433AT14GENIChomozygous108781808
1258213438258213439TC15GENIChomozygous108781815
1258229164258229165TC13GENIChomozygous108624231
1258229221258229222TG14GENIChomozygous108781817
1258234923258234924CG28GENIChomozygous108624237
1258234936258234937CT28GENIChomozygous108624238
1258235912258235913TC26GENIChomozygous108781822
1258236608258236609TA19GENIChomozygous108781823
1258237067258237068CT10GENIChomozygous108781824
1258237260258237261CT8GENIChomozygous108781825
1258237262258237263TC7GENIChomozygous108781826
1258238426258238427TC17GENIChomozygous108781827
1258238951258238952AC24GENIChomozygous108781828
1258241226258241227TC17GENIChomozygous108781829
1258242653258242654TC23GENIChomozygous108781830
1258244103258244104CT20GENIChomozygous108781831
1258244696258244697GA18GENIChomozygous108781832