| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:33285683-33285954 | Common:1; Rare:60 | ||||
| chr13:33818045-33818197 | Rare:69 | ||||
| chr13:36345535-36345658 | Common:1; Rare:24 | ||||
| chr13:36346269-36346454 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:36999281-36999465 | Rare:73 | ||||
| chr13:37000748-37000815 | Rare:31; Clinvar (pathogenic):1 | ||||
| chr13:37059585-37059757 | Common:1; Rare:56 | ||||
| chr13:37598607-37598972 | Common:2; Rare:99 | ||||
| chr13:37869765-37869967 | Common:1; Rare:50 | ||||
| chr13:39038094-39038465 | Common:1; Rare:90 | ||||
| chr13:39603114-39603286 | Common:1; Rare:57 | ||||
| chr13:40771133-40771427 | Common:3; Rare:90 | ||||
| chr13:40789338-40789621 | Common:2; Rare:97; Clinvar:5; Clinvar (benign):2 | ||||
| chr13:41060924-41061025 | Common:10; Rare:58 | ||||
| chr13:41061152-41061645 | Common:4; Rare:167 |