| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:178153835-178154091 | Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:178204326-178204534 | Common:3; Rare:73 | ||||
| chr5:178627009-178627235 | Common:7; Rare:80 | ||||
| chr5:178859753-178859996 | Common:1; Rare:70 | ||||
| chr5:179550522-179550860 | Common:2; Rare:156 | ||||
| chr5:179559534-179559781 | Common:1; Rare:67 | ||||
| chr5:179623599-179623991 | Common:4; Rare:139 | ||||
| chr5:179698548-179699091 | Common:4; Rare:191 | ||||
| chr5:179858797-179859031 | Rare:123 | ||||
| chr5:179907837-179908021 | Common:2; Rare:99 | ||||
| chr5:180809813-180809976 | Common:4; Rare:39 | ||||
| chr5:180810126-180810280 | Common:4; Rare:46 | ||||
| chr5:180861150-180861435 | Common:2; Rare:115 | ||||
| chr5:181052743-181053119 | Common:6; Rare:116 | ||||
| chr5:181223075-181223313 | Rare:81 |