| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:76047756-76048212 | Common:3; Rare:134 | ||||
| chr7:76282507-76282703 | Common:1; Rare:50 | ||||
| chr7:76302462-76303066 | Common:3; Rare:244; Clinvar:17; Clinvar (benign):13; Clinvar (pathogenic):5 | ||||
| chr7:76303657-76304007 | Common:3; Rare:169; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):7 | ||||
| chr7:76358723-76359145 | Common:1; Rare:154 | ||||
| chr7:76409618-76409873 | Common:2; Rare:60 | ||||
| chr7:77536838-77537191 | Common:4; Rare:103 | ||||
| chr7:77537204-77537589 | Common:4; Rare:98 | ||||
| chr7:77537939-77538096 | Common:4; Rare:60 | ||||
| chr7:77538345-77538592 | Rare:68 | ||||
| chr7:77696186-77696494 | Common:1; Rare:128 | ||||
| chr7:77696825-77697051 | Rare:94 | ||||
| chr7:77697340-77697360 | Rare:3 | ||||
| chr7:77798286-77798919 | Common:1; Rare:148 | ||||
| chr7:79453794-79454046 | Common:2; Rare:62 |