| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24141486-24141771 | Common:2; Rare:71 | ||||
| chr14:24146564-24146680 | Rare:45 | ||||
| chr14:24171802-24172115 | Common:3; Rare:73 | ||||
| chr14:24195400-24195739 | Common:2; Rare:74 | ||||
| chr14:24213444-24213529 | Rare:31 | ||||
| chr14:24215958-24216183 | Common:1; Rare:73 | ||||
| chr14:24232260-24232949 | Common:9; Rare:165 | ||||
| chr14:24242580-24242727 | Common:1; Rare:30; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24299743-24299854 | Common:2; Rare:32 | ||||
| chr14:24429861-24429959 | Rare:22 | ||||
| chr14:24442668-24443028 | Common:5; Rare:114 | ||||
| chr14:26596591-26596732 | Rare:25 | ||||
| chr14:26597303-26597741 | Common:2; Rare:97 | ||||
| chr14:31025375-31025662 | Common:2; Rare:65 | ||||
| chr14:31420524-31420763 | Common:3; Rare:71 |