| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58228865-58228945 | Rare:25 | ||||
| chr19:58278595-58278998 | Common:4; Rare:126 | ||||
| chr19:58326870-58327021 | Common:1; Rare:31 | ||||
| chr19:58327231-58327304 | Rare:17 | ||||
| chr19:58347483-58347773 | Common:7; Rare:131 | ||||
| chr19:58440134-58440457 | Common:6; Rare:88 | ||||
| chr19:58499222-58499538 | Common:2; Rare:98; Clinvar:2 | ||||
| chr19:58573524-58573701 | Common:3; Rare:48 | ||||
| chr2:677358-677517 | Common:1; Rare:62 | ||||
| chr2:1744452-1744626 | Common:1; Rare:62 | ||||
| chr2:3379624-3379762 | Common:1; Rare:55 | ||||
| chr2:3519485-3519636 | Common:2; Rare:51 | ||||
| chr2:3558220-3558688 | Common:6; Rare:177 | ||||
| chr2:3575107-3575447 | Common:2; Rare:98; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:9423155-9423302 | Common:1; Rare:30 |