chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
165096871550968716GA67GENIChomozygous139941301
165097038150970382AG61GENIChomozygous139941302
165097132150971322AC60GENIChomozygous139941303
165097160950971610CT66GENIChomozygous139941304
165097378950973790T18GENICheterozygous403398605
165097378950973790TC18GENICpossibly homozygous403398606
165097379150973792T18GENICheterozygous403398607
165097379150973792TC18GENICpossibly homozygous403398608
165097508650975087TC52GENIChomozygous139941305
165097571850975719CG6GENICheterozygous139941306
165097573250975733GC6GENICheterozygous139941307
165097603650976036TGTA15GENIChomozygous139837168
165097620050976200TGTGTGTGTGTGTATGTCTGTGTGTATG22GENIChomozygous139837170
165097611850976118TG19GENIChomozygous139837169
165097566250975666GTAT8GENIChomozygous139837167
165097698850976988TA69GENIChomozygous139837171
165097699350976994CA70GENIChomozygous139941308
165097894550978946AG64GENIChomozygous139941309
165097964550979646TG59GENICheterozygous139941310
165098097050980971AG17GENIChomozygous139941311
165098097050980971A20GENICheterozygous403398609
165098152250981523TA47GENIChomozygous139941312
165098306750983068TC56GENIChomozygous139941313
165098337650983377AG61GENIChomozygous139941314
165098604650986047AG44GENIChomozygous139941315
165098875850988759CA19GENICheterozygous139941316
165099082750990828A57GENIChomozygous139837172
165099148250991483TC63GENIChomozygous139941317
165099222250992223T57GENIChomozygous139837173
165099286950992870AC59GENIChomozygous139941318
165099421550994216TG45GENIChomozygous139941319
165099428550994286CT41GENIChomozygous139941320
165099428950994290AG40GENIChomozygous139941321
165099582250995823GA48GENIChomozygous139941322
165099623650996237TC40GENIChomozygous139941323
165099633850996339CT45GENIChomozygous139941324
165099661650996616G27GENICpossibly homozygous139837174
165099749050997491CT45GENIChomozygous139941325
165099752650997527CT44GENIChomozygous139941326