chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228120300228120301CT22GENIChomozygous109000205
1228124368228124369CG35GENIChomozygous109000206
1228124837228124838AG27GENIChomozygous109000207
1228125124228125125TC24GENIChomozygous109000208
1228127327228127328CT9GENIChomozygous109000209
1228127699228127700TA23GENIChomozygous109000210
1228128779228128780CA20GENIChomozygous109000211
1228129114228129115AT27GENIChomozygous109000212
1228131905228131906AC25GENIChomozygous120491507
1228132167228132168AG28GENIChomozygous109000213
1228132278228132279GA34GENIChomozygous109000214