chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8107471370107471371CT14GENICheterozygous154538758
8107471370107471371C14GENICpossibly homozygous403248379
8107471372107471373C14GENICpossibly homozygous403898041
8107471372107471373CT14GENICheterozygous403898042
8107475268107475269T16GENIChomozygous138263310
8107478418107478418C21GENIChomozygous138263311
8107482244107482245T17GENICheterozygous403248380
8107482321107482321TGTTT25GENICpossibly homozygous138263312
8107484526107484527AT7GENIChomozygous403248381
8107484526107484527A7GENICheterozygous403248382
8107482244107482245TC17GENIChomozygous138410154
8107486675107486676GA19GENIChomozygous138410155
8107475683107475684AT21GENIChomozygous138410152
8107478533107478534AT29GENIChomozygous138410153
8107486675107486676G19GENICheterozygous403248383
8107492403107492404CT16GENIChomozygous138410156
8107494376107494377TG21GENIChomozygous138410157
8107496877107496878TC16GENIChomozygous138410158
8107505897107505898TC25GENIChomozygous138410159
8107507063107507064GT13GENIChomozygous138410160
8107509478107509479TC22GENIChomozygous138410161
8107509587107509588TC19GENIChomozygous138410162
8107512910107512911TC19GENIChomozygous138410163
8107516679107516679GAGG8GENIChomozygous138263313
8107519666107519667T28GENICpossibly homozygous138263314
8107520619107520620GA21GENIChomozygous138410164
8107523440107523441GT25GENIChomozygous138410165
8107524734107524735CG19GENIChomozygous138410166
8107526497107526498TC14GENIChomozygous138410167
8107526849107526850TC21GENIChomozygous138410168
8107527791107527792TA25GENIChomozygous138410169
8107531327107531328CT33GENIChomozygous138410170
8107534901107534902T23GENIChomozygous138263315
8107535553107535554GT20GENIChomozygous138410171
8107536012107536013GA23GENIChomozygous138410172
8107537290107537291CT29GENIChomozygous138410173
8107538820107538820GACAAG19GENIChomozygous138263316
8107540593107540593A14GENIChomozygous138263317
8107506441107506446GGTTC4GENICheterozygous149229272