| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24146582-24146694 | Rare:40 | ||||
| chr14:24171942-24172088 | Common:1; Rare:36 | ||||
| chr14:24195339-24195360 | Rare:7 | ||||
| chr14:24195391-24195729 | Common:2; Rare:76 | ||||
| chr14:24213433-24213622 | Common:1; Rare:61 | ||||
| chr14:24232312-24232531 | Common:8; Rare:52 | ||||
| chr14:24232847-24232954 | Rare:25 | ||||
| chr14:24242264-24242433 | Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24242586-24242781 | Common:1; Rare:50; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24271460-24271552 | Rare:31 | ||||
| chr14:24271554-24271903 | Common:3; Rare:77 | ||||
| chr14:24299712-24299873 | Common:4; Rare:46 | ||||
| chr14:24399104-24399255 | Rare:47 | ||||
| chr14:24429852-24429980 | Rare:31 | ||||
| chr14:24442644-24443023 | Common:6; Rare:121 |