chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186898612168986122TC23GENIChomozygous110396214
186898651668986517CA26GENICpossibly homozygous110396216
186899796468997965CT25GENIChomozygous110396218
186899810468998105AG24GENIChomozygous110396220
186899868468998685TA28GENICpossibly homozygous110396222
186899868568998686CA27GENIChomozygous110396224
186899870768998708CT25GENIChomozygous110396226
186899876268998763AT27GENIChomozygous110396228
186899909468999095AG21GENIChomozygous110396230
186899925268999253CG14GENIChomozygous110396232
186899953068999531AT30GENIChomozygous110396234
186899987668999877AG19GENIChomozygous110396236
186899988368999884TC19GENIChomozygous110396238
186900146769001468CT28GENIChomozygous110396240
186900167069001671CT15GENIChomozygous119500191
186900172069001721TC11GENIChomozygous119500193
186900182569001826CT9GENIChomozygous119549049
186900202269002023TG22GENIChomozygous119500194
186900222769002228TG23GENIChomozygous119500196
186900237269002373GA12GENIChomozygous119549051
186900332369003324TC28GENIChomozygous110396242
186900354569003546GA26GENIChomozygous110396244
186900418169004182TC17GENIChomozygous110396246