| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179698686-179699072 | Common:2; Rare:128 | ||||
| chr5:179806884-179807056 | Common:3; Rare:64 | ||||
| chr5:179820710-179820949 | Common:6; Rare:96; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:179858792-179859025 | Rare:122 | ||||
| chr5:180072128-180072225 | Common:1; Rare:42 | ||||
| chr5:180353321-180353491 | Common:4; Rare:70 | ||||
| chr5:180802756-180802953 | Common:6; Rare:82 | ||||
| chr5:180803876-180804004 | Common:2; Rare:29 | ||||
| chr5:180810121-180810219 | Common:1; Rare:20 | ||||
| chr5:181040121-181040293 | Rare:34 | ||||
| chr5:181223122-181223313 | Rare:65 | ||||
| chr5:181223529-181223733 | Common:3; Rare:47 | ||||
| chr5:181243685-181243948 | Common:4; Rare:96 | ||||
| chr5:181261060-181261274 | Rare:73 | ||||
| chr6:292448-292542 | Rare:31 |