chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95421291354212914TC20GENIChomozygous117342040
95421385354213854TC25GENIChomozygous117342041
95422693354226934TA28GENIChomozygous117342042
95423054154230542CG14GENIChomozygous117342043
95423161754231618TG25GENICpossibly homozygous117342044
95423189354231894CT8GENIChomozygous117342045
95423266154232662GA8GENIChomozygous117342046
95423366354233664TA17GENIChomozygous117342048
95423487554234876CT25GENIChomozygous117342049
95423540454235405CT9GENIChomozygous117342050
95423730554237306AG10GENIChomozygous117342051
95423929054239291TG16GENIChomozygous117342052
95424084254240843AT20GENIChomozygous117342053
95424214554242146CA15GENIChomozygous117342054
95424457454244575CT24GENIChomozygous117342055
95424462054244621AC16GENIChomozygous117342056
95424618454246185AG12GENIChomozygous117342057
95424996554249966CG9GENIChomozygous117342058
95425030754250308TG9GENIChomozygous117342059
95425154154251542AG10GENIChomozygous117342060
95425159954251600GA9GENIChomozygous117342061
95425160554251606CT9GENIChomozygous117342062
95425381854253819TC12GENIChomozygous117342063
95425431654254317TC18GENIChomozygous117342064
95425443754254438CT18GENIChomozygous117342065
95425518454255185AG14GENIChomozygous117342066
95425537654255377TA13GENICpossibly homozygous117342067
95425811754258118TC19GENIChomozygous117342069
95425957754259578CT18GENIChomozygous117342071
95426647454266475TC19GENIChomozygous117342073
95426760154267602GC10GENIChomozygous117342074
95426816154268162TC18GENIChomozygous117342075
95426937654269377GA19GENIChomozygous117342076
95427808554278086CT17GENIChomozygous117531964
95427967754279678AG26GENIChomozygous117342077
95428045154280452CT15GENIChomozygous117342078
95428256654282567AG20GENIChomozygous117342079
95428347954283480TC21GENIChomozygous117342080
95428465054284651AG46GENIChomozygous117531966
95428441354284414AG32GENIChomozygous117342082