chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116371048116371049AC24GENIChomozygous116669113
8116372305116372306CT9GENICheterozygous126674925
8116373060116373061GA16GENICheterozygous126674927
8116373091116373092CT13GENIChomozygous126674928
8116373100116373101CT11GENICheterozygous126674929
8116373998116373999TC23GENIChomozygous116669115
8116374290116374291CT14GENIChomozygous116669117
8116374344116374345AC20GENIChomozygous116669119
8116374711116374712TC20GENIChomozygous116669121
8116374894116374895GA21GENIChomozygous116669123
8116374962116374963AG10GENIChomozygous116669125
8116374976116374977CG11GENIChomozygous116669127
8116377878116377879TA9GENIChomozygous116669141
8116378976116378977GA16GENIChomozygous116669145
8116379424116379425AC21GENIChomozygous116669147
8116379895116379896TA27GENIChomozygous116669149
8116380205116380206GT18GENIChomozygous116669151
8116380657116380658TC23GENIChomozygous116669153
8116380670116380671AG18GENIChomozygous116669155
8116380846116380847TC23GENIChomozygous116669157
8116380881116380882AG4GENIChomozygous116669159
8116381176116381177GA21GENIChomozygous116669161
8116381260116381261GA20GENIChomozygous116669163
8116381577116381578AG19GENIChomozygous116669165
8116381652116381653CT15GENIChomozygous116669167
8116381760116381761TC24GENIChomozygous116669169
8116382042116382043CT16GENIChomozygous116669173
8116382077116382078GA7GENIChomozygous116669175
8116383487116383488GA27GENIChomozygous116669177
8116384688116384689AG10GENIChomozygous116669183
8116384693116384694AT6GENIChomozygous116669185
8116384694116384695CG6GENIChomozygous116669187
8116385400116385401TC27GENIChomozygous116669189
8116386724116386725AG10GENIChomozygous116669191
8116386945116386946CG19GENIChomozygous116669193
8116387506116387507GA30GENIChomozygous116669195
8116378410116378411TG14GENICheterozygous116886427
8116380873116380874GA3GENICheterozygous116886429