chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108285711282857113CT41GENIChomozygous970468220
108285741782857418AG32GENIChomozygous970468221
108286236582862366GA40GENICpossibly homozygous970468222
108286267982862680GA20GENIChomozygous970468223
108286281782862818GA8GENIChomozygous970468224
108286282682862827GA9GENIChomozygous970468225
108286310982863110AG30GENIChomozygous970468226
108286317982863180CT26GENIChomozygous970468227
108286370182863702GT16GENIChomozygous970468228
108286483982864840CT27GENIChomozygous970468229
108286490782864908TC36GENIChomozygous970468230
108286515682865157TA32GENIChomozygous970468231
108286541782865418AT25GENIChomozygous970468232
108286568482865685AG46GENIChomozygous970468233
108286574582865746GA44GENIChomozygous970468234
108286601382866014TA38GENIChomozygous970468235
108286657682866577GA38GENIChomozygous970468236
108286668982866690GA39GENIChomozygous970468237
108286678882866789GA37GENIChomozygous970468238
108286726182867262CT25GENIChomozygous970468239
108286734482867345TC28GENIChomozygous970468240
108286779682867797GA38GENIChomozygous970468241
108286803682868037CA47GENIChomozygous970468242
108286844082868441GA34GENIChomozygous970468243
108286876782868768CT41GENIChomozygous970468244
108286934082869341CT31GENIChomozygous970468245
108286952682869527AC47GENIChomozygous970468246
108286971082869711TC41GENIChomozygous970468247
108287094582870946TC21GENIChomozygous970468248
108287119982871200CT13GENIChomozygous970468249
108287120482871205CT13GENIChomozygous970468250
108288397882883979CT42GENIChomozygous970468251
108288769582887696CG24GENIChomozygous970468252