| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24213567-24213654 | Common:2; Rare:24 | ||||
| chr14:24232295-24232714 | Common:8; Rare:104 | ||||
| chr14:24232832-24232968 | Rare:33 | ||||
| chr14:24242280-24242433 | Rare:51; Clinvar (benign):2 | ||||
| chr14:24242544-24242732 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:24299707-24299858 | Common:4; Rare:44 | ||||
| chr14:24367839-24368203 | Common:2; Rare:63 | ||||
| chr14:24429842-24429980 | Common:1; Rare:35 | ||||
| chr14:24442659-24443048 | Common:5; Rare:122 | ||||
| chr14:26597416-26597628 | Common:1; Rare:40 | ||||
| chr14:30559109-30559197 | Common:1; Rare:31 | ||||
| chr14:30622211-30622344 | Rare:48 | ||||
| chr14:31025413-31025664 | Common:2; Rare:57 | ||||
| chr14:31207473-31207870 | Common:2; Rare:131 | ||||
| chr14:31420541-31420763 | Common:2; Rare:68 |