| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:75985836-75986018 | Common:4; Rare:80; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:75994489-75994772 | Common:4; Rare:139 | ||||
| chr7:76047927-76048226 | Common:2; Rare:105 | ||||
| chr7:76302451-76302754 | Common:3; Rare:114; Clinvar:6; Clinvar (benign):6 | ||||
| chr7:76302877-76303024 | Rare:69; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr7:76303026-76303075 | Rare:14; Clinvar (benign):1 | ||||
| chr7:76625666-76625985 | Common:5; Rare:89 | ||||
| chr7:76627248-76627358 | Common:5; Rare:31 | ||||
| chr7:77122036-77122268 | Common:2; Rare:49 | ||||
| chr7:77122281-77122664 | Common:2; Rare:76 | ||||
| chr7:77199732-77199894 | Rare:46 | ||||
| chr7:77537910-77538073 | Common:4; Rare:65 | ||||
| chr7:77696189-77696500 | Common:1; Rare:134 | ||||
| chr7:77696757-77697032 | Rare:122 | ||||
| chr7:77798320-77798980 | Common:1; Rare:155 |