| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73926689-73927019 | Common:4; Rare:296; Clinvar:20; Clinvar (benign):6 | ||||
| chr2:73985800-73986160 | Common:5; Rare:149 | ||||
| chr2:74147830-74148045 | Common:2; Rare:112; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:74178703-74179087 | Common:9; Rare:199 | ||||
| chr2:74198434-74198645 | Rare:165 | ||||
| chr2:74391793-74392143 | Common:4; Rare:301 | ||||
| chr2:74421579-74421842 | Rare:163 | ||||
| chr2:74440350-74440675 | Rare:134 | ||||
| chr2:74454778-74455159 | Rare:188 | ||||
| chr2:74455336-74456218 | Common:1; Rare:416 | ||||
| chr2:74457930-74458457 | Common:2; Rare:179 | ||||
| chr2:74465247-74465508 | Common:2; Rare:131; Clinvar:2; Clinvar (benign):4 | ||||
| chr2:74472360-74473100 | Common:8; Rare:396 | ||||
| chr2:74482854-74483110 | Common:2; Rare:136 | ||||
| chr2:74502860-74503260 | Common:2; Rare:109 |