Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73851715-73851974 | Common:4; Rare:85 | ||||
chr14:73886773-73886905 | Common:2; Rare:45 | ||||
chr14:73950107-73950328 | Common:5; Rare:87; Clinvar (benign):3 | ||||
chr14:74019254-74019428 | Common:1; Rare:68 | ||||
chr14:74493252-74493777 | Common:4; Rare:168; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr14:74713049-74713207 | Rare:89 | ||||
chr14:74881622-74881967 | Common:1; Rare:121 | ||||
chr14:75002741-75003017 | Common:1; Rare:95; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr14:75127001-75127120 | Rare:38 | ||||
chr14:75660800-75661371 | Common:5; Rare:142 | ||||
chr14:76151735-76151972 | Rare:89 | ||||
chr14:77097980-77098282 | Rare:93 | ||||
chr14:77320859-77321099 | Rare:73; Clinvar:1 | ||||
chr14:77377049-77377449 | Common:2; Rare:125 | ||||
chr14:77457523-77458166 | Common:2; Rare:185 |