chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135651331256513313AC26GENIChomozygous114357628
135651608656516087GT28GENIChomozygous114357630
135651674356516744AG39GENIChomozygous114553966
135652178056521781AT22GENIChomozygous114357632
135652191456521915GC16GENIChomozygous114357638
135652282156522822GA28GENIChomozygous114357640
135652285856522859GA34GENIChomozygous114357642
135652372356523724TG15GENIChomozygous114357644
135652373256523733GA14GENIChomozygous114357646
135652378856523789CG20GENIChomozygous114357648
135652509656525097TC26GENIChomozygous114357650
135652743756527438AG25GENIChomozygous114357652
135652763456527635GT24GENIChomozygous114357654
135652776056527761GA24GENICpossibly homozygous114357658
135652798356527984AG16GENIChomozygous114357660
135652770956527710AG25GENICheterozygous118452181
135653289356532894AT23GENIChomozygous114357662
135654163556541636CT20GENIChomozygous114357664