| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:79406227-79406334 | Common:3; Rare:34 | ||||
| chr13:80339275-80339332 | Common:1; Rare:12 | ||||
| chr13:93226563-93226897 | Common:2; Rare:68; Clinvar (benign):1 | ||||
| chr13:93226915-93227113 | Rare:37; Clinvar:1 | ||||
| chr13:93227177-93227436 | Rare:62; Clinvar:5 | ||||
| chr13:94596092-94596338 | Common:2; Rare:90 | ||||
| chr13:95301403-95301526 | Rare:35 | ||||
| chr13:96053338-96053487 | Common:2; Rare:66 | ||||
| chr13:97222109-97222497 | Rare:75 | ||||
| chr13:97433978-97434200 | Rare:89 | ||||
| chr13:98143945-98144059 | Rare:33 | ||||
| chr13:99200668-99200900 | Common:6; Rare:109 | ||||
| chr13:100088808-100089135 | Rare:128; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr13:100674753-100675056 | Common:3; Rare:122 | ||||
| chr13:102596772-102597035 | Common:1; Rare:122 |