| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103521300-103521990 | Common:6; Rare:335; Clinvar:2 | ||||
| chr14:103528999-103529279 | Common:2; Rare:134 | ||||
| chr14:103562565-103563255 | Common:22; Rare:553; Clinvar:2; Clinvar (benign):18 | ||||
| chr14:103629081-103629238 | Rare:147 | ||||
| chr14:103715387-103715854 | Common:2; Rare:307 | ||||
| chr14:103847525-103847792 | Common:5; Rare:178 | ||||
| chr14:103921469-103921711 | Common:3; Rare:77 | ||||
| chr14:103928262-103928540 | Common:4; Rare:171 | ||||
| chr14:104138234-104138610 | Common:6; Rare:242 | ||||
| chr14:104689413-104689690 | Common:3; Rare:118; Clinvar (benign):2 | ||||
| chr14:104724058-104724254 | Common:4; Rare:139 | ||||
| chr14:104724490-104724880 | Common:2; Rare:87 | ||||
| chr14:104736386-104737000 | Common:8; Rare:173 | ||||
| chr14:104752600-104753234 | Common:7; Rare:270 | ||||
| chr14:104795678-104795964 | Rare:135 |