| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:76302877-76303073 | Rare:83; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr7:76303456-76303821 | Common:2; Rare:155; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:76303965-76303994 | Rare:14; Clinvar (benign):2 | ||||
| chr7:76358919-76359145 | Rare:97 | ||||
| chr7:76397427-76397569 | Rare:57 | ||||
| chr7:76627233-76627372 | Common:5; Rare:44 | ||||
| chr7:77122281-77122302 | Rare:4 | ||||
| chr7:77122320-77122638 | Common:2; Rare:67 | ||||
| chr7:77696133-77696520 | Common:1; Rare:156 | ||||
| chr7:77798334-77798910 | Common:1; Rare:141 | ||||
| chr7:79453546-79453721 | Rare:43 | ||||
| chr7:79453742-79454123 | Common:3; Rare:93 | ||||
| chr7:80134509-80134945 | Common:4; Rare:136 | ||||
| chr7:80135656-80136018 | Rare:91 | ||||
| chr7:80602148-80602356 | Common:1; Rare:43; Clinvar:6; Clinvar (benign):1 |