| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103130900-103131280 | Common:6; Rare:114 | ||||
| chr14:103333373-103333686 | Common:1; Rare:132 | ||||
| chr14:103333819-103334348 | Common:12; Rare:570 | ||||
| chr14:103334625-103334872 | Common:2; Rare:205 | ||||
| chr14:103335413-103335767 | Common:2; Rare:164 | ||||
| chr14:103385142-103385579 | Common:3; Rare:351 | ||||
| chr14:103385710-103386150 | Common:2; Rare:154 | ||||
| chr14:103521054-103521343 | Common:3; Rare:237 | ||||
| chr14:103521419-103521683 | Common:2; Rare:141 | ||||
| chr14:103522766-103523137 | Common:1; Rare:158 | ||||
| chr14:103528954-103529358 | Common:4; Rare:248 | ||||
| chr14:103561223-103562098 | Common:11; Rare:284 | ||||
| chr14:103562007-103562407 | Rare:322 | ||||
| chr14:103562528-103563338 | Common:33; Rare:931; Clinvar:3; Clinvar (benign):27 | ||||
| chr14:103628830-103629679 | Common:18; Rare:573 |