| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:149129545-149129711 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377594-149377811 | Common:1; Rare:54 | ||||
| chr3:150408736-150409002 | Rare:82 | ||||
| chr3:150603162-150603401 | Common:2; Rare:98 | ||||
| chr3:152268842-152268958 | Rare:41 | ||||
| chr3:155870379-155870718 | Common:1; Rare:99 | ||||
| chr3:156555080-156555318 | Common:1; Rare:93 | ||||
| chr3:156674362-156674651 | Common:3; Rare:85 | ||||
| chr3:157160090-157160327 | Rare:100 | ||||
| chr3:157543233-157543340 | Rare:24 | ||||
| chr3:158644500-158644621 | Common:3; Rare:47; Clinvar (benign):4 | ||||
| chr3:158801991-158802146 | Common:2; Rare:74 | ||||
| chr3:160399196-160399307 | Rare:30; Clinvar:1 | ||||
| chr3:160399518-160399687 | Rare:37 | ||||
| chr3:160449706-160450053 | Common:2; Rare:122 |