| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:75537790-75538144 | Common:3; Rare:110 | ||||
| chr13:75549410-75549823 | Common:8; Rare:109 | ||||
| chr13:77027151-77027327 | Common:6; Rare:58 | ||||
| chr13:77697370-77697687 | Common:2; Rare:83 | ||||
| chr13:77918800-77918887 | Rare:17 | ||||
| chr13:79405797-79405898 | Rare:33 | ||||
| chr13:79406227-79406306 | Common:1; Rare:24 | ||||
| chr13:83882262-83882453 | Rare:41; Clinvar:1 | ||||
| chr13:94596139-94596357 | Common:2; Rare:72 | ||||
| chr13:95676924-95677176 | Common:3; Rare:87 | ||||
| chr13:96053336-96053490 | Common:2; Rare:67 | ||||
| chr13:97222154-97222338 | Rare:35 | ||||
| chr13:98143952-98144214 | Common:3; Rare:63 | ||||
| chr13:99200668-99200900 | Common:6; Rare:109 | ||||
| chr13:100088858-100089134 | Rare:105; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 |