| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:43690817-43691013 | Common:4; Rare:108; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:44477641-44477746 | Common:1; Rare:21 | ||||
| chr3:44624933-44625184 | Common:3; Rare:71 | ||||
| chr3:44761590-44761863 | Common:3; Rare:99 | ||||
| chr3:44861802-44861932 | Common:2; Rare:61 | ||||
| chr3:44976113-44976320 | Common:3; Rare:89 | ||||
| chr3:45594665-45594688 | Rare:5 | ||||
| chr3:45689177-45689459 | Common:1; Rare:94 | ||||
| chr3:45842058-45842287 | Common:1; Rare:61 | ||||
| chr3:46976721-46977005 | Common:3; Rare:63 | ||||
| chr3:46979551-46979868 | Common:2; Rare:78; Clinvar:2 | ||||
| chr3:47164069-47164405 | Rare:79 | ||||
| chr3:47380820-47381072 | Rare:76 | ||||
| chr3:47381436-47381668 | Rare:51 | ||||
| chr3:47475776-47476071 | Common:3; Rare:116 |