| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:75994489-75994772 | Common:4; Rare:139 | ||||
| chr7:76047915-76048191 | Common:2; Rare:96 | ||||
| chr7:76302481-76302706 | Common:2; Rare:79; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:76302810-76303075 | Rare:115; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr7:76303483-76303817 | Common:2; Rare:142; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:77122281-77122699 | Common:2; Rare:84 | ||||
| chr7:77199789-77199907 | Rare:29 | ||||
| chr7:77696122-77696495 | Common:1; Rare:145 | ||||
| chr7:77697055-77697164 | Common:1; Rare:36 | ||||
| chr7:77798344-77798910 | Common:1; Rare:137 | ||||
| chr7:77798914-77798971 | Rare:8 | ||||
| chr7:79453597-79453766 | Common:1; Rare:46 | ||||
| chr7:79453795-79453885 | Common:1; Rare:18 | ||||
| chr7:79453891-79454117 | Common:1; Rare:56 | ||||
| chr7:80134589-80134908 | Common:3; Rare:110 |