| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:50081845-50082341 | Common:2; Rare:137 | ||||
| chr13:50082664-50082835 | Rare:44 | ||||
| chr13:50401256-50401434 | Rare:30 | ||||
| chr13:50909643-50909874 | Common:1; Rare:47; Clinvar:3; Clinvar (benign):1 | ||||
| chr13:50909956-50910435 | Common:2; Rare:127; Clinvar:3 | ||||
| chr13:51222260-51222429 | Common:2; Rare:63 | ||||
| chr13:51451262-51451276 | Rare:3 | ||||
| chr13:51451561-51452068 | Common:2; Rare:165 | ||||
| chr13:51452088-51452108 | Rare:7 | ||||
| chr13:51452625-51452867 | Rare:61 | ||||
| chr13:51452883-51453430 | Common:1; Rare:199 | ||||
| chr13:51453513-51453613 | Common:1; Rare:27 | ||||
| chr13:51453666-51453776 | Common:1; Rare:25 | ||||
| chr13:51454108-51454206 | Rare:26 | ||||
| chr13:51583792-51583975 | Common:1; Rare:43 |