| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24213052-24213170 | Rare:19 | ||||
| chr14:24213394-24213612 | Common:1; Rare:73 | ||||
| chr14:24232249-24232707 | Common:8; Rare:116 | ||||
| chr14:24232820-24232972 | Common:1; Rare:36 | ||||
| chr14:24242258-24242429 | Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24242593-24242669 | Rare:18; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:24271444-24271893 | Common:3; Rare:110 | ||||
| chr14:24299711-24299918 | Common:5; Rare:71 | ||||
| chr14:24429855-24430085 | Common:1; Rare:47 | ||||
| chr14:24442235-24443073 | Common:10; Rare:264 | ||||
| chr14:26597438-26597595 | Common:1; Rare:32 | ||||
| chr14:30622214-30622395 | Common:1; Rare:90 | ||||
| chr14:30874415-30874579 | Rare:59 | ||||
| chr14:31025431-31025755 | Common:3; Rare:87 | ||||
| chr14:31026367-31026670 | Common:4; Rare:94 |