chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95530764855307649GT29GENIChomozygous138598551
95530831255308313TC33GENIChomozygous147358559
95531024755310248TC27GENIChomozygous147358560
95531120455311205GA12GENIChomozygous147358561
95531784455317845AG21GENIChomozygous138598556
95531910555319106AC39GENIChomozygous138598558
95531046155310462C22GENIChomozygous147357739
95532019655320196G29GENIChomozygous138465163
95532604855326050AT28GENICpossibly homozygous138465165
95532746655327467TC24GENIChomozygous138598563
95532799355327994C30GENIChomozygous147357740
95532799555327996C30GENIChomozygous138465166
95533255755332558CT39GENIChomozygous147358562
95533356955333570CT29GENIChomozygous147358563
95533391555333915T31GENIChomozygous147357741
95533407755334078CT20GENIChomozygous147358564
95533762155337622CA28GENIChomozygous147358565
95533804655338047TC44GENIChomozygous138598576
95532799755327998C31GENICheterozygous148537842
95532799755327998CA31GENIChomozygous154577483