| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:25428107-25428424 | Rare:72 | ||||
| chr3:25783388-25783640 | Common:2; Rare:80; Clinvar (benign):3 | ||||
| chr3:25790008-25790130 | Common:4; Rare:48 | ||||
| chr3:28348612-28348724 | Rare:27 | ||||
| chr3:28348779-28349182 | Common:3; Rare:128 | ||||
| chr3:29280999-29281102 | Common:1; Rare:18 | ||||
| chr3:31533016-31533305 | Common:1; Rare:89; Clinvar (benign):2 | ||||
| chr3:31981633-31981780 | Rare:40 | ||||
| chr3:32106402-32106714 | Common:4; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32570651-32570919 | Rare:126 | ||||
| chr3:33277313-33277495 | Common:1; Rare:50 | ||||
| chr3:33798497-33798700 | Common:2; Rare:75 | ||||
| chr3:36993057-36993589 | Common:2; Rare:187; Clinvar:35; Clinvar (benign):15; Clinvar (pathogenic):4 | ||||
| chr3:37243188-37243474 | Common:1; Rare:69 | ||||
| chr3:38024510-38024652 | Common:1; Rare:52 |