| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:39037761-39037869 | Rare:35 | ||||
| chr13:39038079-39038508 | Common:1; Rare:103 | ||||
| chr13:39603099-39603286 | Common:1; Rare:63 | ||||
| chr13:39655619-39655802 | Common:2; Rare:91; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr13:40667074-40667296 | Rare:34 | ||||
| chr13:40771025-40771264 | Common:1; Rare:88 | ||||
| chr13:40789368-40789635 | Common:2; Rare:89; Clinvar:6; Clinvar (benign):2 | ||||
| chr13:40982836-40982970 | Common:2; Rare:21 | ||||
| chr13:41060814-41061075 | Common:17; Rare:153 | ||||
| chr13:41061126-41061645 | Common:4; Rare:175 | ||||
| chr13:41061701-41061849 | Common:1; Rare:57 | ||||
| chr13:41132719-41133008 | Rare:75 | ||||
| chr13:41194454-41194583 | Common:2; Rare:29 | ||||
| chr13:41311142-41311369 | Common:2; Rare:91 | ||||
| chr13:41457315-41457552 | Common:2; Rare:68 |