| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:73683419-73683626 | Common:3; Rare:85 | ||||
| chr7:73738778-73739017 | Common:1; Rare:75 | ||||
| chr7:74254346-74254517 | Rare:77 | ||||
| chr7:74657453-74657714 | Common:2; Rare:81 | ||||
| chr7:75914911-75915164 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:76047950-76048188 | Common:2; Rare:81 | ||||
| chr7:76302862-76303073 | Rare:89; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr7:76303659-76303865 | Common:1; Rare:93; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
| chr7:77199786-77199980 | Common:1; Rare:41 | ||||
| chr7:77696221-77696467 | Rare:98 | ||||
| chr7:77697064-77697167 | Common:1; Rare:34 | ||||
| chr7:77798343-77798969 | Common:1; Rare:148 | ||||
| chr7:79453612-79454106 | Common:3; Rare:121 | ||||
| chr7:80134635-80134935 | Common:3; Rare:103 | ||||
| chr7:87152314-87152468 | Common:1; Rare:49 |