| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:99876114-99876321 | Common:1; Rare:56 | ||||
| chr3:100260662-100261057 | Rare:114 | ||||
| chr3:100261256-100261460 | Common:1; Rare:43 | ||||
| chr3:100334538-100334829 | Common:2; Rare:103 | ||||
| chr3:100334983-100335069 | Rare:27 | ||||
| chr3:100401004-100401219 | Rare:60 | ||||
| chr3:100401369-100401802 | Common:2; Rare:93 | ||||
| chr3:100401948-100402004 | Rare:5 | ||||
| chr3:100492360-100492675 | Common:2; Rare:105 | ||||
| chr3:100709193-100709702 | Common:9; Rare:153; Clinvar (benign):1 | ||||
| chr3:101512709-101513002 | Common:2; Rare:61 | ||||
| chr3:101513096-101513377 | Common:8; Rare:75 | ||||
| chr3:101513511-101513577 | Rare:16 | ||||
| chr3:101561709-101561962 | Common:2; Rare:92 | ||||
| chr3:101573665-101573826 | Rare:40 |