| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58558703-58559213 | Common:4; Rare:283 | ||||
| chr19:58573276-58573677 | Common:3; Rare:167 | ||||
| chr2:46480-46828 | Common:4; Rare:190 | ||||
| chr2:46800-47130 | Common:2; Rare:111 | ||||
| chr2:264560-265010 | Common:8; Rare:336 | ||||
| chr2:677356-677577 | Common:2; Rare:184 | ||||
| chr2:1744457-1744668 | Common:3; Rare:133 | ||||
| chr2:3377119-3377455 | Common:2; Rare:61 | ||||
| chr2:3377779-3378016 | Common:1; Rare:118 | ||||
| chr2:3379590-3379848 | Common:4; Rare:185 | ||||
| chr2:3518800-3519279 | Common:5; Rare:248 | ||||
| chr2:3519381-3519674 | Common:5; Rare:128 | ||||
| chr2:3558168-3558725 | Common:12; Rare:388 | ||||
| chr2:3575080-3575407 | Common:4; Rare:182; Clinvar:6; Clinvar (benign):12 | ||||
| chr2:8678490-8679300 | Common:21; Rare:464 |