chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95421385354213854TC25GENIChomozygous117342041
95422693354226934TA31GENIChomozygous117342042
95423054154230542CG36GENIChomozygous117342043
95423161754231618TG18GENIChomozygous117342044
95423189354231894CT21GENIChomozygous117342045
95423266154232662GA28GENIChomozygous117342046
95423332454233325AG25GENIChomozygous117342047
95423366354233664TA29GENICpossibly homozygous117342048
95423540454235405CT19GENIChomozygous117342050
95423730554237306AG21GENIChomozygous117342051
95423929054239291TG28GENIChomozygous117342052
95424084254240843AT29GENIChomozygous117342053
95424214554242146CA26GENIChomozygous117342054
95424457454244575CT19GENIChomozygous117342055
95424462054244621AC29GENIChomozygous117342056
95424618454246185AG34GENIChomozygous117342057
95425030754250308TG24GENIChomozygous117342059
95425154154251542AG30GENIChomozygous117342060
95425159954251600GA22GENIChomozygous117342061
95425160554251606CT23GENIChomozygous117342062
95425381854253819TC23GENIChomozygous117342063
95425431654254317TC31GENIChomozygous117342064
95425443754254438CT26GENIChomozygous117342065
95425518454255185AG28GENIChomozygous117342066
95425537654255377TA33GENIChomozygous117342067
95425768054257681GA30GENIChomozygous117342068
95425811754258118TC28GENIChomozygous117342069
95425950554259506AG27GENIChomozygous117342070
95425957754259578CT21GENIChomozygous117342071
95426085554260856AG16GENICpossibly homozygous117549467
95426154254261543GT33GENIChomozygous117342072
95426647454266475TC27GENIChomozygous117342073
95426760154267602GC7GENIChomozygous117342074
95426816154268162TC28GENIChomozygous117342075
95426937654269377GA28GENIChomozygous117342076
95427967754279678AG25GENIChomozygous117342077
95428045154280452CT24GENIChomozygous117342078
95428256654282567AG36GENIChomozygous117342079
95428347954283480TC21GENIChomozygous117342080
95428422754284228CT29GENIChomozygous117342081
95428441354284414AG20GENIChomozygous117342082