chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10104461603104461604CT26GENIChomozygous117030960
10104462160104462161CG32GENIChomozygous117030962
10104462517104462518GA26GENICheterozygous118087457
10104463164104463165TC40GENIChomozygous116835615
10104464129104464130GA29GENIChomozygous116835617
10104464239104464240GA31GENIChomozygous117030964
10104464252104464253CG28GENIChomozygous117030966
10104469085104469086GA32GENIChomozygous117030968
10104469697104469698GA37GENIChomozygous117030970
10104469780104469781TG36GENICheterozygous117260709