| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:36346263-36346454 | Common:2; Rare:51; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:36346622-36346804 | Common:4; Rare:53 | ||||
| chr13:36999292-36999457 | Rare:64 | ||||
| chr13:37000246-37000403 | Common:2; Rare:30 | ||||
| chr13:37000725-37000815 | Rare:37; Clinvar (pathogenic):1 | ||||
| chr13:37006817-37007071 | Common:2; Rare:71; Clinvar (benign):1 | ||||
| chr13:37059585-37059758 | Common:1; Rare:57 | ||||
| chr13:38349540-38349915 | Common:4; Rare:125; Clinvar (pathogenic):1 | ||||
| chr13:38350217-38350291 | Rare:36 | ||||
| chr13:38686899-38687055 | Common:2; Rare:39 | ||||
| chr13:39038081-39038653 | Common:2; Rare:152 | ||||
| chr13:39603120-39603284 | Common:1; Rare:55 | ||||
| chr13:39655627-39655802 | Common:2; Rare:88; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr13:40771125-40771346 | Common:3; Rare:75 | ||||
| chr13:40789361-40789635 | Common:2; Rare:93; Clinvar:6; Clinvar (benign):2 |