chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5134767598134767599TC2GENIChomozygous114144130
5134767638134767639GT4GENIChomozygous114442134
5134773217134773218GA4GENIChomozygous114442136
5134775365134775366TC9GENIChomozygous114144133
5134776988134776989CA9GENICpossibly homozygous114442138
5134781539134781540GA6GENIChomozygous114442144
5134782255134782256AG7GENIChomozygous114017286
5134782287134782288GA10GENIChomozygous114442146
5134783535134783536TC4GENIChomozygous114442150
5134784510134784511CG7GENIChomozygous114017287
5134785010134785011GA6GENIChomozygous114017289