| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129439819-129440345 | Common:1; Rare:162; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129893539-129893875 | Rare:132 | ||||
| chr3:130746796-130746934 | Common:3; Rare:40 | ||||
| chr3:130893912-130894262 | Common:3; Rare:102 | ||||
| chr3:131026720-131026947 | Common:2; Rare:56 | ||||
| chr3:131381464-131381901 | Common:3; Rare:131 | ||||
| chr3:131502819-131502995 | Common:1; Rare:83 | ||||
| chr3:132417155-132417482 | Common:5; Rare:105 | ||||
| chr3:132659799-132659950 | Common:3; Rare:35 | ||||
| chr3:132722102-132722207 | Common:1; Rare:44; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:133661854-133662011 | Rare:35 | ||||
| chr3:134374400-134374674 | Common:1; Rare:78 | ||||
| chr3:134485407-134485772 | Rare:90 | ||||
| chr3:134485957-134486453 | Common:6; Rare:164 | ||||
| chr3:136196562-136196768 | Rare:61 |