chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95421385354213854TC24GENIChomozygous117342041
95422693354226934TA29GENIChomozygous117342042
95423054154230542CG26GENIChomozygous117342043
95423161754231618TG32GENIChomozygous117342044
95423189354231894CT32GENIChomozygous117342045
95423266154232662GA43GENIChomozygous117342046
95423332454233325AG30GENIChomozygous117342047
95423366354233664TA26GENIChomozygous117342048
95423540454235405CT26GENIChomozygous117342050
95423730554237306AG35GENIChomozygous117342051
95423929054239291TG29GENIChomozygous117342052
95424084254240843AT35GENIChomozygous117342053
95424214554242146CA24GENIChomozygous117342054
95424457454244575CT15GENIChomozygous117342055
95425030754250308TG27GENIChomozygous117342059
95424462054244621AC21GENIChomozygous117342056
95424618454246185AG28GENIChomozygous117342057
95425154154251542AG41GENIChomozygous117342060
95425159954251600GA30GENIChomozygous117342061
95425160554251606CT28GENIChomozygous117342062
95425381854253819TC28GENIChomozygous117342063
95425431654254317TC23GENIChomozygous117342064
95425443754254438CT50GENIChomozygous117342065
95425518454255185AG32GENICpossibly homozygous117342066
95425537654255377TA32GENIChomozygous117342067
95425768054257681GA39GENIChomozygous117342068
95425811754258118TC33GENIChomozygous117342069
95425950554259506AG30GENIChomozygous117342070
95425957754259578CT41GENICpossibly homozygous117342071
95426085554260856AG19GENICpossibly homozygous117549467
95426154254261543GT36GENIChomozygous117342072
95426647454266475TC32GENIChomozygous117342073
95426816154268162TC38GENIChomozygous117342075
95426937654269377GA39GENIChomozygous117342076
95427967754279678AG30GENIChomozygous117342077
95428045154280452CT26GENIChomozygous117342078
95428256654282567AG29GENIChomozygous117342079
95428347954283480TC19GENIChomozygous117342080
95428422754284228CT30GENIChomozygous117342081
95428441354284414AG12GENIChomozygous117342082