chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141410870514108706AT8GENIChomozygous113351463
141411388214113883CT15GENIChomozygous114180548
141411430214114303AG20GENIChomozygous113351465
141412075014120751CT21GENIChomozygous113351479
141412096414120965CT12GENIChomozygous113351481
141412103814121039CT5GENIChomozygous113351483
141412127514121276AG20GENIChomozygous113351487
141412321414123215GA13GENIChomozygous113907778
141412346414123465TC10GENIChomozygous114180551
141412425014124251GC12GENIChomozygous113807114
141412444414124445AG11GENIChomozygous113659181
141412570014125701CT28GENIChomozygous113659185
141412621114126212CG10GENIChomozygous113807118
141412883614128837AT6GENIChomozygous113807124
141412949614129497GA13GENIChomozygous113807126