| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:159263256-159263326 | Common:1; Rare:21 | ||||
| chr5:163437292-163437628 | Rare:99 | ||||
| chr5:172771180-172771433 | Common:4; Rare:108 | ||||
| chr5:173328415-173328596 | Rare:34 | ||||
| chr5:176361762-176361947 | Common:2; Rare:46 | ||||
| chr5:176388569-176388798 | Common:4; Rare:85 | ||||
| chr5:177022468-177022741 | Common:2; Rare:95 | ||||
| chr5:177133499-177133844 | Rare:127 | ||||
| chr5:177516932-177517252 | Common:1; Rare:97; Clinvar (pathogenic):1 | ||||
| chr5:178153835-178154090 | Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:178859850-178860052 | Common:1; Rare:61 | ||||
| chr5:179698686-179699056 | Common:2; Rare:121 | ||||
| chr5:179858797-179858977 | Rare:100 | ||||
| chr5:181223169-181223287 | Rare:41 | ||||
| chr5:181243690-181243862 | Common:2; Rare:52 |