chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141005837210058373AG26GENIChomozygous991846304
141005839310058394AC26GENIChomozygous991846305
141005854510058546CA33GENIChomozygous991846306
141005858910058590CT33GENIChomozygous991846307
141005869510058696CT24GENIChomozygous991846308
141005889610058897GA30GENIChomozygous991846309
141005934910059350GA18GENIChomozygous991846310
141006074310060744CT24GENIChomozygous991846311
141006082010060821AG16GENIChomozygous991846312
141006096610060967CT17GENIChomozygous991846313
141006108710061088GC30GENIChomozygous991846314
141006114010061141CT27GENIChomozygous991846315
141006114210061143AT26GENIChomozygous991846316
141006115310061154TC25GENIChomozygous991846317
141006119810061199GA24GENIChomozygous991846318
141006141410061415AC20GENIChomozygous991846319
141006142010061421GA18GENIChomozygous991846320
141006142310061424TA19GENIChomozygous991846321
141006144610061447CA23GENIChomozygous991846322
141006157910061580AG23GENIChomozygous991846323
141006158510061586AG22GENIChomozygous991846324
141006159510061596GA19GENIChomozygous991846325
141006163110061632CT12GENIChomozygous991846326
141006168610061687TC9GENIChomozygous991846327
141006169310061694AG11GENIChomozygous991846328
141006169410061695AG12GENIChomozygous991846329
141006170010061701CT14GENIChomozygous991846330
141006187310061874GA21GENIChomozygous991846331
141006187510061876CA21GENIChomozygous991846332