chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8107470604107470604A10GENIChomozygous145648059
8107475268107475269T17GENIChomozygous138263310
8107478418107478418C7GENIChomozygous138263311
8107482237107482241ACAT16GENIChomozygous145648060
8107486675107486676G17GENICheterozygous403248383
8107480940107480941TC14GENIChomozygous145674171
8107492359107492360CT15GENIChomozygous142099346
8107492200107492201GA18GENIChomozygous145674172
8107478533107478534AT16GENIChomozygous138410153
8107486675107486676GA17GENIChomozygous138410155
8107494376107494377TG17GENIChomozygous138410157
8107496368107496368ATT17GENIChomozygous145648061
8107496877107496878TC18GENIChomozygous138410158
8107505897107505898TC14GENIChomozygous138410159
8107507063107507064GT11GENIChomozygous138410160
8107507302107507303GA20GENIChomozygous145674173
8107509478107509479TC16GENIChomozygous138410161
8107509587107509588TC16GENIChomozygous138410162
8107510365107510366CT7GENIChomozygous145674174
8107512910107512911TC23GENIChomozygous138410163
8107520619107520620GA23GENIChomozygous138410164
8107523440107523441GT14GENIChomozygous138410165
8107526497107526498TC17GENIChomozygous138410167
8107527791107527792TA22GENIChomozygous138410169
8107531327107531328CT23GENIChomozygous138410170
8107532663107532664TC16GENIChomozygous142099388
8107534901107534902T28GENIChomozygous138263315
8107535553107535554GT19GENIChomozygous138410171
8107535668107535669AC23GENIChomozygous145674175
8107536012107536013GA5GENIChomozygous138410172
8107538820107538820GACAAG22GENIChomozygous138263316
8107540593107540593A14GENICpossibly homozygous138263317