| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179806845-179807063 | Common:3; Rare:83 | ||||
| chr5:179820761-179821065 | Common:3; Rare:120; Clinvar:6; Clinvar (benign):2 | ||||
| chr5:179858792-179858958 | Rare:94 | ||||
| chr5:179907703-179908015 | Common:2; Rare:130 | ||||
| chr5:180802766-180802976 | Common:8; Rare:83 | ||||
| chr5:180810108-180810223 | Common:1; Rare:25 | ||||
| chr5:180861208-180861619 | Common:4; Rare:132 | ||||
| chr5:181040110-181040293 | Rare:35 | ||||
| chr5:181052752-181053093 | Common:6; Rare:106 | ||||
| chr5:181203905-181204041 | Common:1; Rare:33 | ||||
| chr5:181205119-181205297 | Common:1; Rare:44 | ||||
| chr5:181223126-181223332 | Rare:74 | ||||
| chr5:181223642-181223855 | Common:4; Rare:48 | ||||
| chr5:181243685-181243960 | Common:4; Rare:98 | ||||
| chr5:181261081-181261234 | Rare:53 |