| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179550255-179550872 | Common:4; Rare:234 | ||||
| chr5:179617499-179618076 | Rare:143 | ||||
| chr5:179618277-179618394 | Common:1; Rare:40 | ||||
| chr5:179621552-179621947 | Common:3; Rare:125 | ||||
| chr5:179622141-179622243 | Common:2; Rare:33 | ||||
| chr5:179623593-179623963 | Common:4; Rare:135 | ||||
| chr5:179698609-179699101 | Common:4; Rare:176 | ||||
| chr5:179806318-179806485 | Rare:58 | ||||
| chr5:179806808-179807107 | Common:3; Rare:103 | ||||
| chr5:179821046-179821424 | Common:2; Rare:111; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:179822473-179822870 | Common:1; Rare:99 | ||||
| chr5:179858792-179858997 | Rare:112 | ||||
| chr5:179907774-179907923 | Common:1; Rare:68 | ||||
| chr5:180291851-180292212 | Common:2; Rare:136 | ||||
| chr5:180330743-180330939 | Rare:51 |