chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103514492035144921GC21GENIChomozygous985844892
103514505035145051CT19GENIChomozygous985844893
103514977935149780AC21GENIChomozygous985844894
103514994035149941AT24GENIChomozygous985844895
103515197435151975CT26GENIChomozygous985844896
103515249035152491CA25GENIChomozygous985844897
103515273435152735AG17GENIChomozygous985844898
103515500635155007CT20GENIChomozygous985844899
103515570535155706AT23GENIChomozygous985844900
103515579735155798AT29GENIChomozygous985844901
103515595035155951GA18GENIChomozygous985844902
103515611535156116TC20GENIChomozygous985844903
103515631935156320TG10GENIChomozygous985844904
103515633135156332GA7GENIChomozygous985844905
103515718435157185GA14GENIChomozygous985844906
103515754935157550AG29GENIChomozygous985844907
103515933635159337TC11GENIChomozygous985844908
103516325535163256CT24GENIChomozygous985844909
103516334035163341TC21GENIChomozygous985844910
103516384635163847AG23GENIChomozygous985844911
103516424235164243CT12GENIChomozygous985844912
103516499835164999TC5GENIChomozygous985844913
103516584235165843AG20GENIChomozygous985844914
103516619035166191AG12GENIChomozygous985844915
103516644935166450AG8GENIChomozygous985844916
103516688935166890CT10GENIChomozygous985844917
103516768235167683CA24GENIChomozygous985844918
103517117535171176AG17GENIChomozygous985844919
103517258035172581TG19GENIChomozygous985844920
103517493035174931GA17GENIChomozygous985844921
103517513035175131AC23GENIChomozygous985844922
103517515435175155AG28GENIChomozygous985844923
103517582635175827TC22GENIChomozygous985844924
103518152835181529CT29GENIChomozygous985844925
103518331835183319AG28GENIChomozygous985844926
103518390035183901AC11GENIChomozygous985844927
103518446335184464CG17GENIChomozygous985844928
103518747335187474CT14GENIChomozygous985844929