| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:102120055-102120254 | Rare:78 | ||||
| chr12:103930367-103930582 | Common:4; Rare:91 | ||||
| chr12:103957135-103957294 | Common:3; Rare:49 | ||||
| chr12:103965691-103965927 | Common:2; Rare:62 | ||||
| chr12:104064322-104064563 | Common:1; Rare:59 | ||||
| chr12:104288854-104289026 | Rare:69 | ||||
| chr12:105236041-105236338 | Common:2; Rare:135 | ||||
| chr12:106247368-106247553 | Common:2; Rare:45 | ||||
| chr12:106955534-106955966 | Rare:157 | ||||
| chr12:108560847-108560922 | Rare:25 | ||||
| chr12:108561138-108561415 | Common:2; Rare:70 | ||||
| chr12:109477268-109477648 | Common:3; Rare:99 | ||||
| chr12:109573487-109573853 | Common:3; Rare:103; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:109880453-109880675 | Common:1; Rare:60 | ||||
| chr12:109996242-109996439 | Common:2; Rare:61 |