| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43545871-43546160 | Common:2; Rare:45 | ||||
| chr17:43546299-43546673 | Common:2; Rare:84 | ||||
| chr17:43578803-43579256 | Common:2; Rare:92 | ||||
| chr17:43579399-43579489 | Common:1; Rare:12 | ||||
| chr17:43579518-43579934 | Common:3; Rare:64 | ||||
| chr17:43778203-43778585 | Rare:80 | ||||
| chr17:43778612-43779203 | Common:4; Rare:160 | ||||
| chr17:43833060-43833202 | Rare:35 | ||||
| chr17:43900565-43900792 | Rare:81 | ||||
| chr17:44005811-44006026 | Rare:67; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:44014872-44015158 | Common:2; Rare:87 | ||||
| chr17:44066228-44066407 | Rare:52 | ||||
| chr17:44066593-44066843 | Common:1; Rare:93 | ||||
| chr17:44070562-44071025 | Common:3; Rare:152; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:44071062-44071185 | Rare:48; Clinvar:2; Clinvar (pathogenic):4 |