| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:52576824-52577271 | Common:6; Rare:164 | ||||
| chr6:56542833-56543119 | Common:2; Rare:43 | ||||
| chr6:63572234-63572569 | Rare:123 | ||||
| chr6:70668079-70668137 | Rare:18 | ||||
| chr6:73263192-73263279 | Common:2; Rare:23 | ||||
| chr6:73394602-73394902 | Common:4; Rare:95 | ||||
| chr6:73461683-73461857 | Common:1; Rare:67; Clinvar (benign):2 | ||||
| chr6:73653914-73654123 | Common:2; Rare:53; Clinvar:3 | ||||
| chr6:73696143-73696226 | Rare:22 | ||||
| chr6:75284728-75284986 | Common:1; Rare:75 | ||||
| chr6:82247709-82247859 | Common:1; Rare:48 | ||||
| chr6:83193187-83193408 | Common:3; Rare:74 | ||||
| chr6:85449524-85449806 | Common:2; Rare:68 | ||||
| chr6:87589946-87590175 | Common:3; Rare:107; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:89638447-89638524 | Common:1; Rare:15 |