chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8118556582118556583TG2GENIChomozygous53368182
8118556691118556692GA18GENICpossibly homozygous52832875
8118556845118556846AG23GENICpossibly homozygous52832876
8118557553118557554GA18GENICpossibly homozygous52832879
8118557881118557882AG10GENICheterozygous52832883
8118557936118557937AATT2GENICheterozygous52832884
8118558134118558135TG11GENIChomozygous52832886
8118558151118558152CT8GENIChomozygous52832887
8118558340118558341AG14GENIChomozygous52832891
8118558364118558365GGC9GENIChomozygous52832892
8118558460118558461TC12GENICpossibly homozygous52832893
8118558497118558498AG18GENIChomozygous52832894
8118558560118558561GGAC14GENIChomozygous52832895
8118558729118558730AG18GENIChomozygous52832896
8118558744118558745CA16GENICpossibly homozygous52832897
8118558987118558988AC24GENIChomozygous52832899
8118559355118559356AG10GENICpossibly homozygous52832901
8118559501118559502TC10GENICheterozygous52832902
8118559559118559560TC14GENIChomozygous52832903
8118559642118559643TG13GENIChomozygous52832904
8118560021118560022CT15GENIChomozygous52832908