| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129278730-129278892 | Common:4; Rare:52 | ||||
| chr3:129316242-129316350 | Rare:50 | ||||
| chr3:129439829-129440437 | Common:5; Rare:192; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:129893558-129893891 | Rare:135 | ||||
| chr3:130746763-130746935 | Common:3; Rare:52 | ||||
| chr3:130893895-130894084 | Common:2; Rare:53 | ||||
| chr3:131026716-131026947 | Common:2; Rare:56 | ||||
| chr3:131381479-131381805 | Common:2; Rare:81 | ||||
| chr3:131502814-131503009 | Common:1; Rare:89 | ||||
| chr3:132417177-132417709 | Common:6; Rare:174 | ||||
| chr3:132659790-132659963 | Common:3; Rare:41 | ||||
| chr3:132722102-132722230 | Common:1; Rare:54; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:133573859-133574041 | Rare:66 | ||||
| chr3:133661856-133662024 | Rare:38 | ||||
| chr3:134366981-134367253 | Rare:54 |