| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:52194397-52194542 | Rare:43 | ||||
| chr13:52599881-52600136 | Common:1; Rare:51 | ||||
| chr13:52617322-52617541 | Common:1; Rare:54 | ||||
| chr13:76885086-76885361 | Rare:98 | ||||
| chr13:76885393-76885726 | Common:1; Rare:119 | ||||
| chr13:87671157-87671401 | Common:1; Rare:67 | ||||
| chr13:93227465-93227597 | Rare:56; Clinvar:1 | ||||
| chr13:95790695-95790902 | Rare:41 | ||||
| chr13:99087946-99088236 | Common:3; Rare:58 | ||||
| chr13:102394493-102394660 | Common:1; Rare:63 | ||||
| chr13:109782713-109782998 | Common:7; Rare:122; Clinvar:1 | ||||
| chr13:110174498-110174642 | Rare:53; Clinvar (benign):1 | ||||
| chr13:110187253-110187623 | Rare:68; Clinvar:1 | ||||
| chr13:110205351-110205530 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr13:110307795-110308123 | Common:2; Rare:118 |