| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:74174857-74174971 | Common:1; Rare:24 | ||||
| chr7:74220740-74221170 | Common:2; Rare:174 | ||||
| chr7:74254306-74254535 | Rare:201 | ||||
| chr7:74289305-74289545 | Common:3; Rare:93 | ||||
| chr7:74453692-74454094 | Common:2; Rare:165 | ||||
| chr7:74657429-74657894 | Common:6; Rare:246 | ||||
| chr7:74658300-74658906 | Common:1; Rare:239 | ||||
| chr7:75073380-75073670 | Common:2; Rare:154 | ||||
| chr7:75073688-75073981 | Common:5; Rare:169 | ||||
| chr7:75611723-75611898 | Common:1; Rare:31 | ||||
| chr7:75878817-75879091 | Common:24; Rare:189 | ||||
| chr7:75907150-75907620 | Common:3; Rare:81 | ||||
| chr7:75914898-75915219 | Common:7; Rare:219; Clinvar:6; Clinvar (benign):2 | ||||
| chr7:75983430-75983790 | Common:4; Rare:128; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:75994497-75994815 | Common:10; Rare:305 |