| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103629385-103629463 | Common:2; Rare:31 | ||||
| chr14:103629582-103629825 | Common:4; Rare:74 | ||||
| chr14:103715237-103715906 | Common:2; Rare:211 | ||||
| chr14:103716322-103716388 | Common:1; Rare:11 | ||||
| chr14:103847491-103847859 | Common:5; Rare:151 | ||||
| chr14:103847976-103848036 | Rare:15 | ||||
| chr14:103921420-103921742 | Common:3; Rare:94 | ||||
| chr14:104138290-104138623 | Common:3; Rare:114 | ||||
| chr14:104689168-104689298 | Common:1; Rare:30 | ||||
| chr14:104689301-104689677 | Common:2; Rare:92; Clinvar (benign):1 | ||||
| chr14:104724053-104724270 | Common:3; Rare:81 | ||||
| chr14:104724409-104724463 | Rare:22 | ||||
| chr14:104752541-104752812 | Common:2; Rare:79 | ||||
| chr14:104752947-104753311 | Common:3; Rare:137 | ||||
| chr14:104753713-104753940 | Common:3; Rare:95 |