| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:66682036-66682185 | Common:5; Rare:70 | ||||
| chr7:66921130-66921225 | Rare:34 | ||||
| chr7:73328033-73328180 | Rare:50 | ||||
| chr7:73683419-73683628 | Common:3; Rare:86 | ||||
| chr7:73738758-73739017 | Common:1; Rare:85 | ||||
| chr7:74028038-74028170 | Common:1; Rare:43; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:74254373-74254528 | Rare:71 | ||||
| chr7:74657506-74657738 | Common:2; Rare:69 | ||||
| chr7:75914915-75915179 | Common:3; Rare:91; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75994493-75994772 | Common:4; Rare:137 | ||||
| chr7:76047972-76048180 | Common:1; Rare:64 | ||||
| chr7:76302481-76302715 | Common:2; Rare:85; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:76302877-76303075 | Rare:83; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr7:77122312-77122691 | Common:2; Rare:77 | ||||
| chr7:77199795-77199849 | Rare:18 |