Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:69611458-69611761 | Common:1; Rare:101 | ||||
chr14:70417014-70417112 | Rare:28 | ||||
chr14:71320296-71320487 | Rare:59 | ||||
chr14:73285960-73286073 | Rare:27 | ||||
chr14:73287294-73287511 | Rare:37 | ||||
chr14:73787133-73787379 | Common:2; Rare:87 | ||||
chr14:73851800-73851976 | Common:4; Rare:61 | ||||
chr14:73886785-73886869 | Common:1; Rare:25 | ||||
chr14:73950071-73950333 | Common:6; Rare:110; Clinvar (benign):4 | ||||
chr14:74019254-74019452 | Common:1; Rare:74 | ||||
chr14:74084403-74084791 | Common:7; Rare:95 | ||||
chr14:74493385-74493777 | Common:4; Rare:122; Clinvar (benign):4 | ||||
chr14:74611524-74611711 | Rare:68; Clinvar:1 | ||||
chr14:74612190-74612292 | Rare:23 | ||||
chr14:74713026-74713213 | Common:1; Rare:104 |