| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:75984812-75985206 | Common:4; Rare:172; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr7:75994489-75994773 | Common:4; Rare:140 | ||||
| chr7:76047743-76048226 | Common:4; Rare:142 | ||||
| chr7:76302509-76303077 | Common:3; Rare:235; Clinvar:18; Clinvar (benign):13; Clinvar (pathogenic):5 | ||||
| chr7:76303356-76303629 | Common:4; Rare:105 | ||||
| chr7:76303657-76304140 | Common:3; Rare:232; Clinvar:9; Clinvar (benign):7; Clinvar (pathogenic):12 | ||||
| chr7:76358726-76359125 | Common:1; Rare:145 | ||||
| chr7:76393155-76393333 | Common:1; Rare:60 | ||||
| chr7:76626785-76626816 | Common:2; Rare:6 | ||||
| chr7:77636811-77637048 | Common:2; Rare:40 | ||||
| chr7:77696113-77696500 | Common:1; Rare:153 | ||||
| chr7:77696986-77697191 | Common:2; Rare:69 | ||||
| chr7:77798284-77798992 | Common:1; Rare:161 | ||||
| chr7:79452817-79452860 | Rare:8 | ||||
| chr7:79452863-79453226 | Common:2; Rare:92; Clinvar (benign):2 |