| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179820710-179821085 | Common:6; Rare:137; Clinvar:6; Clinvar (benign):2 | ||||
| chr5:179822730-179822966 | Common:1; Rare:73; Clinvar:1 | ||||
| chr5:179858792-179859031 | Rare:126 | ||||
| chr5:179907823-179908021 | Common:2; Rare:99 | ||||
| chr5:180291908-180292232 | Common:2; Rare:129 | ||||
| chr5:180494202-180494375 | Common:2; Rare:50 | ||||
| chr5:180802775-180802944 | Common:5; Rare:72 | ||||
| chr5:180809819-180809930 | Common:4; Rare:25 | ||||
| chr5:180810108-180810287 | Common:5; Rare:54 | ||||
| chr5:180861128-180861383 | Common:2; Rare:102 | ||||
| chr5:181205132-181205297 | Common:1; Rare:40 | ||||
| chr5:181222053-181222230 | Common:8; Rare:61 | ||||
| chr5:181223102-181223328 | Rare:83 | ||||
| chr5:181223633-181223768 | Common:3; Rare:29 | ||||
| chr5:181243288-181243551 | Common:4; Rare:99 |