| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:8457582-8457741 | Common:2; Rare:48 | ||||
| chr5:43041614-43041755 | Common:2; Rare:22 | ||||
| chr5:60542145-60542418 | Common:1; Rare:52 | ||||
| chr5:72108235-72108352 | Rare:32 | ||||
| chr5:77080558-77080703 | Common:1; Rare:37 | ||||
| chr5:78510331-78510500 | Common:1; Rare:40 | ||||
| chr5:83528525-83528739 | Rare:39 | ||||
| chr5:87383846-87383849 | |||||
| chr5:87393019-87393137 | Common:1; Rare:31 | ||||
| chr5:95959158-95959251 | Rare:15 | ||||
| chr5:123372709-123372860 | Rare:38; Clinvar (benign):1 | ||||
| chr5:138466191-138466466 | Common:1; Rare:48 | ||||
| chr5:138466538-138466941 | Common:1; Rare:86 | ||||
| chr5:138556462-138556880 | Common:1; Rare:126 | ||||
| chr5:138928987-138929308 | Common:1; Rare:74; Clinvar:1 |