| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151410704-151410836 | Common:2; Rare:26 | ||||
| chr7:151877113-151877139 | Rare:6; Clinvar:1 | ||||
| chr7:152025583-152025802 | Rare:87 | ||||
| chr7:152676097-152676316 | Common:2; Rare:99; Clinvar (benign):6 | ||||
| chr7:152759639-152759879 | Common:4; Rare:101 | ||||
| chr7:155644339-155644836 | Common:4; Rare:162 | ||||
| chr7:156640546-156640770 | Common:3; Rare:105 | ||||
| chr7:157336776-157337069 | Common:2; Rare:141; Clinvar:1 | ||||
| chr7:158856419-158856685 | Common:7; Rare:95 | ||||
| chr8:232176-232486 | Common:3; Rare:131 | ||||
| chr8:233030-233169 | Common:1; Rare:33 | ||||
| chr8:731157-731436 | Common:3; Rare:109 | ||||
| chr8:1823741-1824062 | Common:8; Rare:127 | ||||
| chr8:1973826-1973920 | Rare:41 | ||||
| chr8:2127490-2127809 | Common:14; Rare:79 |