| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129439836-129440350 | Common:1; Rare:158; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129893558-129893883 | Rare:131 | ||||
| chr3:130893905-130894231 | Common:3; Rare:96 | ||||
| chr3:131026720-131026955 | Common:2; Rare:59 | ||||
| chr3:131381451-131381843 | Common:3; Rare:111 | ||||
| chr3:131502759-131503016 | Common:1; Rare:104 | ||||
| chr3:132317309-132317534 | Rare:53 | ||||
| chr3:132417169-132417709 | Common:6; Rare:176 | ||||
| chr3:132659799-132659946 | Common:3; Rare:35 | ||||
| chr3:132722137-132722311 | Common:2; Rare:68; Clinvar:12; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:133573809-133574025 | Rare:75 | ||||
| chr3:133661849-133662011 | Rare:37 | ||||
| chr3:134485437-134485772 | Rare:82 | ||||
| chr3:134485957-134486456 | Common:6; Rare:164 | ||||
| chr3:135965563-135965794 | Common:1; Rare:101 |