| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:139344437-139344555 | Rare:21 | ||||
| chr3:139389558-139389853 | Common:1; Rare:99 | ||||
| chr3:140941708-140941870 | Common:1; Rare:56 | ||||
| chr3:141368260-141368535 | Rare:58 | ||||
| chr3:141486920-141487074 | Common:1; Rare:45 | ||||
| chr3:141876489-141876670 | Common:1; Rare:68 | ||||
| chr3:142225550-142225653 | Rare:32 | ||||
| chr3:142447964-142448161 | Common:1; Rare:78 | ||||
| chr3:142578710-142578927 | Rare:73; Clinvar:1 | ||||
| chr3:143001454-143001631 | Common:2; Rare:63 | ||||
| chr3:146160973-146161276 | Common:1; Rare:105; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:146544545-146544827 | Common:4; Rare:66 | ||||
| chr3:149129545-149129692 | Common:1; Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377578-149377699 | Common:1; Rare:24 | ||||
| chr3:150408720-150408992 | Rare:86 |