chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117699920117699921TA29GENIChomozygous117930413
8117699921117699922AG30GENIChomozygous117930414
8117700323117700324AG16GENIChomozygous117059277
8117701145117701146AG29GENIChomozygous116672154
8117701671117701672AG28GENIChomozygous117059279
8117702377117702378CT13GENIChomozygous116672158
8117702413117702414AG16GENIChomozygous116672160
8117706981117706982CT24GENIChomozygous117059281
8117713266117713267AG30GENIChomozygous117059284
8117714603117714604CT20GENIChomozygous117059286
8117714681117714682GA25GENIChomozygous117059288
8117715505117715506AG37GENIChomozygous116672202
8117715842117715843TC21GENIChomozygous116672204
8117716825117716826TC16GENIChomozygous116672208
8117716935117716936CA22GENIChomozygous116672210
8117717055117717056AG22GENIChomozygous116672212
8117718283117718284TC17GENIChomozygous116672220
8117718674117718675GT20GENIChomozygous117059290
8117719789117719790CT29GENIChomozygous117059292
8117720151117720152GA20GENIChomozygous117059294
8117720261117720262CT30GENIChomozygous117059296
8117720757117720758TC25GENIChomozygous116672222
8117721233117721234AG16GENIChomozygous117059298
8117722347117722348TC16GENIChomozygous117059300
8117722469117722470AG16GENIChomozygous117059302
8117722857117722858GA26GENIChomozygous117059303
8117723062117723063CA27GENIChomozygous117059305
8117723251117723252AG24GENICpossibly homozygous116672224
8117723420117723421AG10GENIChomozygous117059307
8117723726117723727GA26GENIChomozygous117059311
8117723950117723951GA30GENIChomozygous117059313
8117724084117724085TC31GENIChomozygous117059315
8117725009117725010CT27GENIChomozygous117059316
8117726095117726096CT29GENIChomozygous117059318