| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:80340832-80341114 | Common:1; Rare:83 | ||||
| chr13:83882267-83882461 | Rare:42; Clinvar:1 | ||||
| chr13:93227192-93227456 | Rare:65; Clinvar:5 | ||||
| chr13:94596144-94596314 | Common:2; Rare:58 | ||||
| chr13:94601541-94601918 | Common:4; Rare:112 | ||||
| chr13:95676828-95677186 | Common:3; Rare:137 | ||||
| chr13:96053344-96053526 | Common:2; Rare:84 | ||||
| chr13:97222141-97222385 | Rare:44 | ||||
| chr13:97434614-97434784 | Rare:25 | ||||
| chr13:98143934-98144203 | Common:3; Rare:62 | ||||
| chr13:99200668-99200900 | Common:6; Rare:109 | ||||
| chr13:99606497-99606698 | Common:5; Rare:59 | ||||
| chr13:100088941-100089123 | Rare:69; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr13:100674778-100675061 | Common:3; Rare:116 | ||||
| chr13:102596804-102597048 | Common:1; Rare:118; Clinvar (benign):1 |