chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96528035365280354TA17GENIChomozygous117579040
96528039165280392TC19GENIChomozygous117579042
96528045165280452AG18GENIChomozygous117579044
96528124565281246CT14GENIChomozygous117579046
96528125765281258GA17GENIChomozygous117579048
96528132865281329GA18GENIChomozygous117579050
96528148065281481TC19GENIChomozygous117579052
96528162265281623GA26GENIChomozygous117579054
96528228865282289TC10GENIChomozygous117366132
96528238565282386GA8GENIChomozygous117579056
96528245065282451GA8GENIChomozygous117579057
96528260365282604CT15GENIChomozygous117579059
96528303565283036GA13GENIChomozygous117579061
96528323965283240GA11GENIChomozygous117579063
96528334765283348GA11GENIChomozygous117579065
96528346865283469GA17GENIChomozygous117579067
96528351465283515CG18GENIChomozygous117579069
96528362365283624GC20GENIChomozygous117579071
96528376765283768TG12GENIChomozygous117579073
96528386665283867GA7GENIChomozygous117579075
96528386765283868CT7GENIChomozygous117579077
96528401765284018TC20GENIChomozygous117579079
96528458765284588CG15GENIChomozygous117579081
96528480865284809CT13GENIChomozygous117579083
96528531665285317CT24GENIChomozygous117579087
96528547365285474CT12GENIChomozygous117579089
96528549065285491GA8GENIChomozygous117579091
96528573765285738AG22GENIChomozygous117579093
96528596865285969AG23GENIChomozygous117579095
96528649965286500CT6GENIChomozygous117579097
96528699165286992GA25GENIChomozygous117579101
96528822265288223CT19GENIChomozygous117579103
96528848365288484CT6GENIChomozygous117579105
96528874565288746TC19GENIChomozygous117579107
96528979265289793GA16GENIChomozygous117579109
96529031365290314TC23GENIChomozygous117579111
96529041665290417AG15GENIChomozygous117366184
96529062965290630AG22GENIChomozygous117579113
96529094265290943GA25GENIChomozygous117579117
96529173065291731CT4GENIChomozygous117366193
96529192965291930TC12GENIChomozygous117579119