| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:157159378-157159725 | Common:6; Rare:113 | ||||
| chr3:157159791-157159928 | Common:1; Rare:36 | ||||
| chr3:157160130-157160327 | Rare:80 | ||||
| chr3:157436721-157437064 | Common:3; Rare:76; Clinvar:1 | ||||
| chr3:157533607-157533817 | Common:2; Rare:30 | ||||
| chr3:157543179-157543466 | Common:1; Rare:64 | ||||
| chr3:158105699-158105893 | Common:5; Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:158672349-158672777 | Common:5; Rare:133 | ||||
| chr3:158732173-158732253 | Common:3; Rare:27 | ||||
| chr3:158732417-158732650 | Common:3; Rare:84 | ||||
| chr3:159764297-159764516 | Common:2; Rare:65 | ||||
| chr3:159988703-159988741 | Rare:6 | ||||
| chr3:160399164-160399307 | Rare:37; Clinvar:2 | ||||
| chr3:160399475-160399715 | Rare:70; Clinvar:2 | ||||
| chr3:160412072-160412374 | Common:1; Rare:90 |