| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:31138553-31138792 | Rare:66 | ||||
| chr13:31162333-31162467 | Common:1; Rare:39 | ||||
| chr13:32315426-32315509 | Rare:21 | ||||
| chr13:33285703-33285887 | Rare:42 | ||||
| chr13:33818043-33818231 | Rare:89 | ||||
| chr13:37000072-37000415 | Common:2; Rare:73 | ||||
| chr13:37000501-37000822 | Common:3; Rare:101; Clinvar (pathogenic):1 | ||||
| chr13:39037865-39038470 | Common:2; Rare:161 | ||||
| chr13:40666579-40666766 | Common:2; Rare:75 | ||||
| chr13:40771127-40771400 | Common:3; Rare:85 | ||||
| chr13:40789349-40789660 | Common:2; Rare:109; Clinvar:6; Clinvar (benign):2 | ||||
| chr13:41060930-41061670 | Common:13; Rare:274 | ||||
| chr13:41132723-41132987 | Rare:72 | ||||
| chr13:41194444-41194613 | Common:2; Rare:37 | ||||
| chr13:41263367-41263412 | Rare:16 |