| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:54567953-54568384 | Common:3; Rare:158 | ||||
| chr14:54754200-54754600 | Common:3; Rare:85 | ||||
| chr14:54754550-54755130 | Common:7; Rare:341 | ||||
| chr14:54755310-54755500 | Rare:75 | ||||
| chr14:54901766-54903115 | Common:16; Rare:815; Clinvar:19; Clinvar (benign):17; Clinvar (pathogenic):11 | ||||
| chr14:55026921-55027321 | Common:12; Rare:495 | ||||
| chr14:55027456-55028237 | Common:3; Rare:221 | ||||
| chr14:55051327-55051788 | Common:4; Rare:987 | ||||
| chr14:55051902-55052586 | Common:8; Rare:518 | ||||
| chr14:55128880-55129380 | Common:2; Rare:171 | ||||
| chr14:55190769-55191163 | Common:1; Rare:72 | ||||
| chr14:55191098-55191885 | Common:41; Rare:629 | ||||
| chr14:55271108-55271508 | Common:8; Rare:409 | ||||
| chr14:55271420-55272360 | Common:20; Rare:722 | ||||
| chr14:55411666-55412861 | Common:20; Rare:819 |