| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128153380-128153491 | Rare:31 | ||||
| chr3:128879408-128879677 | Common:4; Rare:131; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129183814-129184091 | Common:2; Rare:97 | ||||
| chr3:129249555-129249717 | Common:1; Rare:48 | ||||
| chr3:129316284-129316340 | Rare:21 | ||||
| chr3:129439832-129440333 | Common:1; Rare:155; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:131381489-131381814 | Common:2; Rare:84 | ||||
| chr3:131502869-131503039 | Common:1; Rare:65 | ||||
| chr3:132417393-132417594 | Common:2; Rare:73 | ||||
| chr3:132659745-132660031 | Common:3; Rare:62 | ||||
| chr3:133661935-133662009 | Rare:17 | ||||
| chr3:134485701-134485764 | Rare:26 | ||||
| chr3:134485946-134486253 | Common:4; Rare:110 | ||||
| chr3:136752364-136752671 | Common:1; Rare:108 | ||||
| chr3:136862016-136862295 | Common:1; Rare:89 |