| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:90154252-90154327 | Rare:17 | ||||
| chr7:90154363-90154525 | Rare:43 | ||||
| chr7:90211573-90211940 | Common:4; Rare:112 | ||||
| chr7:90245082-90245292 | Common:1; Rare:68 | ||||
| chr7:90346553-90346744 | Common:4; Rare:84 | ||||
| chr7:90595833-90596031 | Common:6; Rare:66 | ||||
| chr7:90596222-90596709 | Common:2; Rare:159 | ||||
| chr7:91880656-91880816 | Common:1; Rare:46 | ||||
| chr7:91940827-91941004 | Common:3; Rare:60; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:92134369-92134860 | Common:5; Rare:142 | ||||
| chr7:92245849-92246438 | Common:6; Rare:180; Clinvar:4; Clinvar (benign):5 | ||||
| chr7:92528367-92528816 | Common:3; Rare:137; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92833906-92834007 | Rare:28 | ||||
| chr7:93117929-93118123 | Rare:31 | ||||
| chr7:93232201-93232395 | Common:2; Rare:34 |