chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117127199117127200GC34GENIChomozygous116670984
8117128934117128935TC20GENICpossibly homozygous117149354
8117129806117129807AC25GENIChomozygous116886934
8117132310117132311GA11GENICpossibly homozygous117149355
8117132828117132829AC23GENIChomozygous116670988
8117133075117133076CT22GENIChomozygous116670990
8117133443117133444TC26GENIChomozygous116670992
8117134088117134089CT30GENIChomozygous116670994
8117134718117134719TC23GENIChomozygous116670998
8117135158117135159TA24GENIChomozygous117149356
8117135229117135230CT31GENIChomozygous116671000
8117135916117135917GA23GENIChomozygous117149357
8117140818117140819GA26GENIChomozygous116671012
8117141666117141667CT28GENIChomozygous117149358
8117142167117142168TC33GENICpossibly homozygous117149359
8117143706117143707GA25GENIChomozygous116671014
8117144080117144081AG20GENIChomozygous116671016
8117148181117148182GA36GENIChomozygous117149360
8117148685117148686GA30GENIChomozygous117149361
8117148691117148692CT28GENIChomozygous116671024
8117149567117149568TA19GENIChomozygous116671026
8117150952117150953GA28GENIChomozygous116671028
8117151888117151889AG23GENIChomozygous117149362
8117153648117153649AT22GENIChomozygous116671034
8117154200117154201TC36GENIChomozygous116671036
8117155793117155794AG20GENIChomozygous116671040
8117156147117156148TC23GENIChomozygous116671042
8117161298117161299CT16GENIChomozygous116671052
8117167217117167218AG13GENIChomozygous116671058
8117167628117167629AG13GENIChomozygous116671062
8117169474117169475GA19GENICpossibly homozygous117149364
8117155363117155364AG17GENIChomozygous118073282