| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128726289-128726356 | Common:1; Rare:14; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:128879360-128879704 | Common:5; Rare:162; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:129122144-129122329 | Rare:21 | ||||
| chr3:129160986-129161129 | Rare:58 | ||||
| chr3:129183672-129184079 | Common:4; Rare:136 | ||||
| chr3:129249518-129249744 | Common:2; Rare:65 | ||||
| chr3:129278730-129279126 | Common:4; Rare:102 | ||||
| chr3:129316210-129316366 | Common:1; Rare:69 | ||||
| chr3:129316696-129317099 | Common:5; Rare:65 | ||||
| chr3:129428608-129428820 | Common:2; Rare:60 | ||||
| chr3:129439754-129440374 | Common:1; Rare:185; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129487901-129488065 | Common:3; Rare:27 | ||||
| chr3:129893580-129893910 | Rare:137 | ||||
| chr3:130746604-130746873 | Common:2; Rare:80 | ||||
| chr3:130893891-130894224 | Common:3; Rare:102 |