| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:23375381-23375905 | Common:12; Rare:326 | ||||
| chr13:23579139-23579551 | Common:10; Rare:185 | ||||
| chr13:23888510-23888966 | Common:2; Rare:178 | ||||
| chr13:23889303-23889707 | Common:2; Rare:329 | ||||
| chr13:24160480-24160800 | Common:2; Rare:176 | ||||
| chr13:24512387-24512519 | Common:1; Rare:36 | ||||
| chr13:24512626-24512977 | Common:19; Rare:303 | ||||
| chr13:24763904-24764319 | Common:8; Rare:356 | ||||
| chr13:24922190-24922661 | Common:12; Rare:188 | ||||
| chr13:24922741-24923691 | Common:19; Rare:991; Clinvar:7; Clinvar (benign):1 | ||||
| chr13:25287290-25287850 | Common:12; Rare:354 | ||||
| chr13:25301320-25301742 | Common:7; Rare:476 | ||||
| chr13:25301730-25302200 | Common:11; Rare:244 | ||||
| chr13:25372260-25372610 | Common:4; Rare:110; Clinvar:1 | ||||
| chr13:26221579-26222063 | Common:3; Rare:471 |