| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:77919397-77919729 | Common:1; Rare:115; Clinvar:2; Clinvar (benign):1 | ||||
| chr13:78659121-78659215 | Common:2; Rare:73 | ||||
| chr13:79405797-79405911 | Rare:39 | ||||
| chr13:79406227-79406339 | Common:3; Rare:36 | ||||
| chr13:79481019-79481435 | Common:2; Rare:161 | ||||
| chr13:83882259-83882461 | Rare:42; Clinvar:1 | ||||
| chr13:91398538-91398708 | Common:3; Rare:75 | ||||
| chr13:93226513-93227075 | Common:2; Rare:111; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:93227246-93227403 | Rare:30; Clinvar:4 | ||||
| chr13:94596118-94596332 | Common:2; Rare:75 | ||||
| chr13:94601568-94601924 | Common:4; Rare:106 | ||||
| chr13:95676911-95677218 | Common:3; Rare:110 | ||||
| chr13:96053327-96053490 | Common:2; Rare:73 | ||||
| chr13:97222190-97222397 | Rare:34 | ||||
| chr13:97434660-97434711 | Rare:7 |