| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:132417197-132417542 | Common:2; Rare:105 | ||||
| chr3:132659799-132659989 | Common:3; Rare:41 | ||||
| chr3:133038187-133038409 | Common:1; Rare:75 | ||||
| chr3:133661837-133662010 | Rare:39 | ||||
| chr3:134374423-134374765 | Common:2; Rare:101 | ||||
| chr3:134485413-134485760 | Rare:84 | ||||
| chr3:134485973-134486253 | Common:3; Rare:95 | ||||
| chr3:136196562-136196609 | Rare:13 | ||||
| chr3:136250315-136250373 | Common:2; Rare:30; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:136752224-136752671 | Common:1; Rare:143 | ||||
| chr3:136862024-136862269 | Common:1; Rare:67 | ||||
| chr3:138115577-138115711 | Common:4; Rare:32 | ||||
| chr3:138594209-138594479 | Rare:85 | ||||
| chr3:139389568-139389868 | Common:1; Rare:96 | ||||
| chr3:139539554-139539814 | Common:3; Rare:81 |