chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266515633266515634GT22GENIChomozygous109028295
1266515698266515699GA26GENIChomozygous109028296
1266517139266517140TC40GENIChomozygous109028298
1266517462266517463TC24GENIChomozygous108638270
1266518615266518616CA16GENIChomozygous109028299
1266518913266518914AG33GENIChomozygous109028300
1266519218266519219AC24GENIChomozygous109028301
1266519441266519442TG17GENIChomozygous109028302
1266519592266519593GA27GENIChomozygous109028303
1266519594266519595GA29GENIChomozygous109028304
1266520103266520104AG24GENIChomozygous109028305
1266520417266520418TG21GENIChomozygous109028306
1266520608266520609AT22GENIChomozygous109028307
1266522446266522447CG21GENIChomozygous109028308
1266522447266522448AG19GENIChomozygous109028309
1266522902266522903GA27GENIChomozygous108784030
1266522992266522993AC20GENIChomozygous108784031
1266523343266523344GA29GENIChomozygous109028310
1266523584266523585GC26GENIChomozygous108784034