chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
177097659270976593GT29GENIChomozygous111085047
177097659470976595TG29GENIChomozygous111085049
177099502170995022AG4GENIChomozygous111503336
177099502970995030GA4GENIChomozygous111503338
177099503070995031AG4GENIChomozygous111360252
177099503770995038AC4GENIChomozygous111503340
177099503870995039CA5GENIChomozygous111503342
177099505670995057CT5GENIChomozygous111465809
177099505770995058TC5GENIChomozygous111465811
177101148471011485AG28GENIChomozygous111085051
177101161871011619CA24GENIChomozygous111085052
177102756271027563CA27GENIChomozygous111085054
177102763571027636TA21GENIChomozygous111085056
177102763971027640CT22GENIChomozygous111085058
177104164371041644TG8GENIChomozygous111212242
177109019771090198AG25GENIChomozygous111085060
177109045671090457CT20GENIChomozygous111085061
177109409371094094TA37GENIChomozygous111212243
177110130971101310GC13GENIChomozygous111212244