| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44467838-44467869 | Common:1; Rare:11 | ||||
| chr7:65750913-65751060 | Common:1; Rare:56 | ||||
| chr7:65770741-65770897 | Common:5; Rare:42 | ||||
| chr7:66493551-66493737 | Common:3; Rare:75 | ||||
| chr7:66592304-66592420 | Common:2; Rare:46 | ||||
| chr7:66654382-66654576 | Common:1; Rare:73 | ||||
| chr7:67302417-67302667 | Common:5; Rare:73 | ||||
| chr7:73005926-73006136 | Rare:13 | ||||
| chr7:94410275-94410437 | Rare:39; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr7:100335899-100336125 | Common:1; Rare:70 | ||||
| chr7:156950570-156950617 | Rare:14 | ||||
| chr9:35684266-35684500 | Rare:47; Clinvar:2; Clinvar (benign):3 | ||||
| chr9:40992009-40992276 | Common:5; Rare:19 | ||||
| chr9:41358803-41358916 | Common:1; Rare:33 | ||||
| chr9:87728101-87728808 | Common:2; Rare:190 |