| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129160995-129161128 | Rare:53 | ||||
| chr3:129183814-129184079 | Common:2; Rare:89 | ||||
| chr3:129249503-129249701 | Common:3; Rare:59 | ||||
| chr3:129316284-129316315 | Rare:17 | ||||
| chr3:129439838-129440401 | Common:1; Rare:171; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:129893585-129893887 | Rare:129 | ||||
| chr3:130893911-130894231 | Common:3; Rare:93 | ||||
| chr3:131026720-131026968 | Common:2; Rare:64 | ||||
| chr3:131381479-131381811 | Common:2; Rare:84 | ||||
| chr3:131502809-131503016 | Common:1; Rare:92 | ||||
| chr3:132417169-132417557 | Common:5; Rare:128 | ||||
| chr3:132659795-132659950 | Common:3; Rare:38 | ||||
| chr3:133661813-133662010 | Rare:47 | ||||
| chr3:134373725-134373810 | Rare:30 | ||||
| chr3:134374360-134374732 | Common:3; Rare:110 |