chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116371048116371049AC9GENIChomozygous116669113
8116373998116373999TC25GENIChomozygous116669115
8116374344116374345AC20GENIChomozygous116669119
8116374711116374712TC22GENIChomozygous116669121
8116374894116374895GA21GENIChomozygous116669123
8116374976116374977CG24GENIChomozygous116669127
8116377155116377156AC22GENIChomozygous116669139
8116377878116377879TA32GENIChomozygous116669141
8116378976116378977GA36GENIChomozygous116669145
8116379424116379425AC32GENIChomozygous116669147
8116379895116379896TA28GENIChomozygous116669149
8116380205116380206GT30GENIChomozygous116669151
8116380657116380658TC27GENIChomozygous116669153
8116380670116380671AG28GENIChomozygous116669155
8116380846116380847TC19GENIChomozygous116669157
8116380872116380873AG13GENIChomozygous117912549
8116380873116380874GA11GENIChomozygous116886429
8116380881116380882AG9GENIChomozygous116669159
8116381176116381177GA32GENIChomozygous116669161
8116381260116381261GA25GENIChomozygous116669163
8116381577116381578AG41GENIChomozygous116669165
8116381652116381653CT20GENIChomozygous116669167
8116381760116381761TC33GENIChomozygous116669169
8116382042116382043CT13GENIChomozygous116669173
8116382077116382078GA20GENIChomozygous116669175
8116383487116383488GA22GENIChomozygous116669177
8116384688116384689AG20GENIChomozygous116669183
8116384693116384694AT14GENIChomozygous116669185
8116384694116384695CG15GENIChomozygous116669187
8116385400116385401TC22GENIChomozygous116669189
8116386724116386725AG10GENIChomozygous116669191
8116386945116386946CG15GENIChomozygous116669193
8116386952116386953CT15GENIChomozygous116988053