| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:38350468-38350661 | Common:2; Rare:33 | ||||
| chr13:39037574-39037740 | Common:1; Rare:56 | ||||
| chr13:39037903-39038472 | Common:2; Rare:150 | ||||
| chr13:39603122-39603290 | Common:1; Rare:58 | ||||
| chr13:40771098-40771490 | Common:3; Rare:120 | ||||
| chr13:40789377-40789655 | Common:2; Rare:97; Clinvar:6; Clinvar (benign):2 | ||||
| chr13:41060842-41061065 | Common:16; Rare:132 | ||||
| chr13:41061126-41061670 | Common:4; Rare:185 | ||||
| chr13:41061680-41061826 | Common:1; Rare:58 | ||||
| chr13:41132705-41132978 | Rare:71 | ||||
| chr13:41194555-41194833 | Rare:61 | ||||
| chr13:41262716-41262985 | Rare:49 | ||||
| chr13:41263037-41263228 | Common:1; Rare:32 | ||||
| chr13:41373312-41373571 | Common:3; Rare:43 | ||||
| chr13:41374080-41374126 | Rare:10 |