| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:95133586-95133928 | Common:3; Rare:109 | ||||
| chr8:95268718-95268844 | Common:7; Rare:30 | ||||
| chr8:95269245-95269519 | Common:10; Rare:87 | ||||
| chr8:96235503-96235652 | Common:1; Rare:78; Clinvar (benign):2 | ||||
| chr8:96261571-96261957 | Common:6; Rare:131 | ||||
| chr8:98045374-98045660 | Common:3; Rare:89 | ||||
| chr8:98117144-98117382 | Common:4; Rare:72 | ||||
| chr8:99013007-99013355 | Rare:74; Clinvar:1 | ||||
| chr8:99893557-99893802 | Common:2; Rare:90 | ||||
| chr8:100150555-100150701 | Rare:47 | ||||
| chr8:100310088-100310296 | Common:1; Rare:84 | ||||
| chr8:100559734-100559881 | Rare:38 | ||||
| chr8:100953311-100953471 | Common:1; Rare:38 | ||||
| chr8:101205532-101205876 | Common:4; Rare:108 | ||||
| chr8:102238832-102239135 | Common:5; Rare:102; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 |