| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24146528-24147060 | Common:3; Rare:157 | ||||
| chr14:24147154-24147562 | Common:2; Rare:106 | ||||
| chr14:24161027-24161377 | Common:2; Rare:72 | ||||
| chr14:24161475-24161810 | Common:2; Rare:80 | ||||
| chr14:24171701-24172114 | Common:5; Rare:97 | ||||
| chr14:24188179-24188418 | Common:1; Rare:78 | ||||
| chr14:24188727-24189032 | Rare:106 | ||||
| chr14:24195534-24196023 | Common:2; Rare:128 | ||||
| chr14:24212993-24213259 | Rare:46 | ||||
| chr14:24213333-24213715 | Common:4; Rare:124 | ||||
| chr14:24215507-24215711 | Common:1; Rare:79 | ||||
| chr14:24215850-24216192 | Common:1; Rare:121 | ||||
| chr14:24232320-24232724 | Common:8; Rare:92 | ||||
| chr14:24232799-24232976 | Common:1; Rare:43 | ||||
| chr14:24242225-24242455 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):3 |