chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104565945245659453GC9GENIChomozygous116584143
104566015145660152GA7GENIChomozygous116584145
104566055945660560CT19GENIChomozygous116584147
104566174145661742TC17GENIChomozygous116584149
104566330245663303TC28GENIChomozygous116584151
104566377545663776AG21GENIChomozygous116584153
104566442745664428TC19GENIChomozygous116584159
104566585345665854TC20GENIChomozygous116584161
104566615345666154GA16GENIChomozygous116584163
104566629145666292TC21GENIChomozygous116584165
104566797845667979GA24GENIChomozygous116584167
104566828945668290TC32GENIChomozygous116584169
104566913645669137TC24GENIChomozygous116584173
104566927245669273AG21GENIChomozygous116584175
104566987345669874GA20GENIChomozygous116584177
104567218545672186AC24GENICpossibly homozygous116877283
104567350245673503TC32GENIChomozygous116584179
104567381745673818CA39GENIChomozygous116877285
104567463345674634AG41GENIChomozygous116584183
104567659045676591AG25GENIChomozygous116584185
104567668745676688AG32GENIChomozygous116584187
104567699645676997AG23GENIChomozygous116771880
104567832145678322TA22GENIChomozygous116584191
104567899645678997TG26GENIChomozygous116584193
104567918145679182GA21GENIChomozygous116771882
104567935845679359TC21GENIChomozygous116771884
104567990445679905AG42GENIChomozygous116771886
104568559245685593GA16GENIChomozygous116771894
104568056945680570CT23GENIChomozygous116771888
104568497545684976CT24GENIChomozygous116771890
104568515945685160GT29GENIChomozygous116771892