| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20469712-20469748 | Rare:11 | ||||
| chr14:20469958-20470137 | Common:1; Rare:28 | ||||
| chr14:20470247-20470322 | Common:1; Rare:11 | ||||
| chr14:20609408-20609563 | Common:3; Rare:57 | ||||
| chr14:20609815-20610130 | Common:3; Rare:86 | ||||
| chr14:20610137-20610231 | Common:1; Rare:78 | ||||
| chr14:20683637-20684014 | Common:8; Rare:86 | ||||
| chr14:20684026-20684279 | Common:12; Rare:117; Clinvar:2; Clinvar (benign):3 | ||||
| chr14:20684423-20684618 | Common:2; Rare:32; Clinvar (benign):2 | ||||
| chr14:20780731-20781248 | Common:5; Rare:80 | ||||
| chr14:20989628-20990080 | Common:8; Rare:117 | ||||
| chr14:20990342-20990503 | Common:2; Rare:61 | ||||
| chr14:21103592-21103831 | Common:1; Rare:51 | ||||
| chr14:21103987-21104334 | Common:2; Rare:79 | ||||
| chr14:21104622-21104721 | Common:2; Rare:13 |