chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145092714145092715GA53GENIChomozygous112870601
4145095105145095106CG44GENICheterozygous112870602
4145095112145095113GA42GENICheterozygous113058853
4145095113145095114GT42GENICheterozygous112870603
4145095121145095122GA51GENICheterozygous112870604
4145095124145095125AG53GENICheterozygous112870605
4145095154145095155GA50GENICheterozygous112870606
4145095188145095189GA58GENICheterozygous112870607
4145095191145095192AG61GENICheterozygous112870608
4145095209145095210GC66GENICheterozygous112870609
4145095221145095222TC68GENICheterozygous112870610
4145095611145095612AT71GENIChomozygous112870611
4145096881145096882CA37GENICpossibly homozygous112870612
4145100240145100241CA52GENIChomozygous112870613
4145104785145104786GA51GENIChomozygous112870614
4145104968145104969TC58GENIChomozygous112870615
4145106184145106185CA49GENIChomozygous112870616
4145106664145106665AG41GENIChomozygous112870617
4145107507145107508AG60GENIChomozygous112870618
4145107650145107651AC68GENIChomozygous112870619
4145108903145108904AT38GENIChomozygous112870620
4145108931145108932CG21GENIChomozygous112870621
4145108936145108937GT20GENICheterozygous112870622
4145108972145108973GA33GENICheterozygous112870623
4145110650145110651GA54GENIChomozygous112870624