| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:73008633-73008938 | Common:1; Rare:117 | ||||
| chr8:73293579-73293869 | Common:1; Rare:104 | ||||
| chr8:73746795-73747105 | Common:3; Rare:87 | ||||
| chr8:73747408-73747430 | Rare:4 | ||||
| chr8:73747436-73747548 | Rare:24 | ||||
| chr8:73878789-73879009 | Common:3; Rare:105 | ||||
| chr8:73972065-73972536 | Common:2; Rare:133 | ||||
| chr8:73976029-73976251 | Common:5; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:74350009-74350063 | Common:1; Rare:5 | ||||
| chr8:74350225-74350577 | Common:2; Rare:131; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr8:74984376-74984679 | Common:3; Rare:107 | ||||
| chr8:76681013-76681161 | Common:2; Rare:35 | ||||
| chr8:76681170-76681395 | Rare:44 | ||||
| chr8:76683084-76683917 | Common:5; Rare:175 | ||||
| chr8:77000029-77000272 | Common:1; Rare:93; Clinvar:5 |