| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:152676128-152676258 | Common:2; Rare:44 | ||||
| chr7:155644377-155644886 | Common:6; Rare:162 | ||||
| chr7:156640535-156640680 | Common:3; Rare:74 | ||||
| chr7:156950130-156950344 | Common:2; Rare:96 | ||||
| chr7:157336770-157336786 | Rare:8 | ||||
| chr7:157336790-157337149 | Common:3; Rare:161; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:158704768-158704975 | Common:1; Rare:74 | ||||
| chr7:158856413-158856685 | Common:7; Rare:95 | ||||
| chr8:232165-232436 | Common:3; Rare:110 | ||||
| chr8:2127577-2127833 | Common:8; Rare:54 | ||||
| chr8:6406533-6406689 | Common:3; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6563240-6563265 | Rare:4 | ||||
| chr8:6708179-6708363 | Common:2; Rare:68 | ||||
| chr8:6877854-6878225 | Common:5; Rare:108 | ||||
| chr8:8702117-8702232 | Common:2; Rare:32 |