| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23321619-23322032 | Common:4; Rare:123; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:23555916-23556446 | Common:4; Rare:125 | ||||
| chr14:23567468-23567573 | Rare:30 | ||||
| chr14:23567745-23567845 | Rare:23 | ||||
| chr14:23953632-23953869 | Common:9; Rare:97 | ||||
| chr14:23954116-23954349 | Common:2; Rare:68 | ||||
| chr14:23988797-23989004 | Common:8; Rare:88 | ||||
| chr14:24094007-24094366 | Common:3; Rare:96 | ||||
| chr14:24115002-24115296 | Common:2; Rare:83 | ||||
| chr14:24141465-24141909 | Common:2; Rare:112 | ||||
| chr14:24146534-24146887 | Common:1; Rare:114 | ||||
| chr14:24147227-24147526 | Common:2; Rare:82 | ||||
| chr14:24179500-24179830 | Common:1; Rare:105 | ||||
| chr14:24183926-24184092 | Common:1; Rare:62 | ||||
| chr14:24195414-24195738 | Common:1; Rare:73 |