chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102902959729029598TC31GENIChomozygous116864753
102903027129030272TG22GENIChomozygous116539016
102903283429032835TG34GENIChomozygous116539018
102903430429034305TA22GENIChomozygous117193039
102903101629031017AG27GENIChomozygous117216918
102903166229031663TC35GENIChomozygous117216920
102903116029031161AT7GENIChomozygous117120932
102903197929031980GA31GENIChomozygous117193035
102903224729032248CT28GENIChomozygous117193036
102903296529032966CT21GENIChomozygous117193037
102903427729034278TG22GENIChomozygous117193038
102903478429034785GA26GENIChomozygous116539020
102903621429036215AG39GENIChomozygous116539024
102903676329036764GA27GENIChomozygous117193040
102903704429037045TC38GENIChomozygous116539026
102903796329037964AG28GENIChomozygous116539032
102903796429037965CT27GENIChomozygous116539034
102903796629037967CT27GENIChomozygous116539036
102903796929037970GA27GENIChomozygous116539038
102904224229042243AG39GENIChomozygous116539058
102904297529042976CT35GENIChomozygous117193041
102904301129043012AT33GENIChomozygous116750941
102904306929043070AT28GENIChomozygous116750947
102904348429043485GA28GENIChomozygous117103042
102904355529043556GT38GENIChomozygous117140699
102904454729044548AG13GENICheterozygous118080342
102904453929044540GA12GENICheterozygous118096271