| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179698614-179699099 | Common:4; Rare:172 | ||||
| chr5:179806312-179806429 | Rare:36 | ||||
| chr5:179806783-179807099 | Common:3; Rare:109 | ||||
| chr5:179823886-179824310 | Common:1; Rare:174; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr5:179858797-179858969 | Rare:96 | ||||
| chr5:179907711-179907923 | Common:1; Rare:82 | ||||
| chr5:180292031-180292180 | Common:1; Rare:45 | ||||
| chr5:180494163-180494471 | Common:2; Rare:112 | ||||
| chr5:180810108-180810242 | Common:1; Rare:34 | ||||
| chr5:181223176-181223309 | Rare:47 | ||||
| chr5:181223562-181223749 | Common:3; Rare:44 | ||||
| chr5:181261060-181261262 | Rare:68 | ||||
| chr6:292002-292335 | Common:1; Rare:56 | ||||
| chr6:693054-693209 | Rare:49 | ||||
| chr6:1389419-1389598 | Rare:33 |