| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:74174093-74174441 | Common:1; Rare:161 | ||||
| chr7:74254379-74254528 | Rare:67 | ||||
| chr7:74453929-74454150 | Rare:62 | ||||
| chr7:74657527-74657794 | Common:2; Rare:73 | ||||
| chr7:74657933-74658067 | Common:1; Rare:30 | ||||
| chr7:75914915-75915189 | Common:3; Rare:99; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:75994484-75994835 | Common:5; Rare:168 | ||||
| chr7:76047950-76048213 | Common:2; Rare:90 | ||||
| chr7:76302513-76303075 | Common:3; Rare:232; Clinvar:17; Clinvar (benign):13; Clinvar (pathogenic):5 | ||||
| chr7:76303771-76303882 | Rare:55; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
| chr7:76627251-76627361 | Common:5; Rare:29 | ||||
| chr7:77122281-77122672 | Common:2; Rare:78 | ||||
| chr7:77199182-77199442 | Rare:82 | ||||
| chr7:77199691-77199777 | Rare:23 | ||||
| chr7:77199779-77199936 | Rare:38 |