| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:46211247-46211410 | Common:3; Rare:22 | ||||
| chr13:46211752-46212034 | Common:2; Rare:82 | ||||
| chr13:46378519-46378630 | Common:2; Rare:20 | ||||
| chr13:46387167-46387352 | Rare:44 | ||||
| chr13:46390008-46390171 | Common:1; Rare:28 | ||||
| chr13:46437636-46437984 | Common:2; Rare:76 | ||||
| chr13:46438067-46438317 | Common:2; Rare:84 | ||||
| chr13:46553077-46553389 | Common:4; Rare:90 | ||||
| chr13:46797094-46797362 | Common:3; Rare:89 | ||||
| chr13:46896852-46896897 | Rare:13 | ||||
| chr13:47945866-47946057 | Common:1; Rare:29 | ||||
| chr13:48001225-48001383 | Common:1; Rare:72; Clinvar:3; Clinvar (benign):6 | ||||
| chr13:48037639-48037676 | Rare:11 | ||||
| chr13:48037677-48037767 | Rare:46 | ||||
| chr13:48037912-48038053 | Common:4; Rare:47 |