| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58544162-58544474 | Common:4; Rare:133 | ||||
| chr19:58549991-58550273 | Common:2; Rare:105 | ||||
| chr19:58554992-58555210 | Common:2; Rare:66 | ||||
| chr19:58558952-58559133 | Common:1; Rare:53 | ||||
| chr19:58564495-58564822 | Rare:61 | ||||
| chr19:58573357-58573795 | Common:5; Rare:104 | ||||
| chr2:264007-264128 | Common:2; Rare:45 | ||||
| chr2:264537-265002 | Common:4; Rare:178 | ||||
| chr2:677358-677557 | Common:1; Rare:84 | ||||
| chr2:3377792-3377994 | Rare:57 | ||||
| chr2:3519525-3519663 | Common:1; Rare:34 | ||||
| chr2:3558269-3558481 | Common:5; Rare:89 | ||||
| chr2:3575107-3575331 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):4 | ||||
| chr2:9423447-9423697 | Rare:82 | ||||
| chr2:9555672-9555966 | Common:2; Rare:101 |