chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31541112315411124CT32GENIChomozygous120077244
31541201915412020GA24GENIChomozygous111881603
31541239515412396AG26GENIChomozygous111454664
31541358315413584CA26GENICpossibly homozygous120077245
31541559215415593AC30GENIChomozygous111454665
31541565015415651CT28GENIChomozygous111454666
31541579215415793AC28GENIChomozygous120077246
31541597715415978CT35GENICpossibly homozygous120077247
31541670915416710GA27GENIChomozygous111454669
31541704415417045TG14GENIChomozygous111454670
31541745315417454AG31GENIChomozygous111454671
31541810615418107AG26GENIChomozygous111454672
31541823715418238AG22GENIChomozygous111454673
31541851515418516CA21GENIChomozygous111454674
31541880815418809TC12GENIChomozygous111454675
31541888115418882GA9GENIChomozygous120077248
31541897315418974GA12GENIChomozygous111881607
31541900115419002TC19GENIChomozygous111454676
31541929715419298TC17GENIChomozygous111454677
31542009015420091TC20GENIChomozygous111454679
31542179715421798CT30GENIChomozygous111881609
31542203515422036AT25GENIChomozygous111881611
31542211815422119TC21GENIChomozygous111881613
31542311215423113GA29GENICpossibly homozygous120077249
31542317115423172CG27GENIChomozygous111881615
31542352815423529CT26GENIChomozygous111881617
31542356415423565GT33GENIChomozygous111881619
31542381915423820GA26GENIChomozygous111881621
31542400915424010CT25GENIChomozygous111881623
31542404815424049GA34GENIChomozygous111454682
31542467015424671CT25GENICpossibly homozygous111881625
31542712515427126CT30GENIChomozygous111881627
31542762415427625TC26GENIChomozygous111454687
31542855615428557TC26GENIChomozygous111454690
31542892515428926GA27GENIChomozygous111881635
31542908815429089CG18GENIChomozygous111454693
31542908915429090GA18GENIChomozygous119697526
31542968415429685AG27GENIChomozygous111454698
31543037215430373GA22GENICpossibly homozygous120077250
31543059115430592GA20GENIChomozygous111454701
31543171815431719TC15GENIChomozygous111454704