| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:68288184-68288641 | Common:4; Rare:126 | ||||
| chr5:68290221-68290383 | Rare:33 | ||||
| chr5:68290530-68290707 | Rare:35 | ||||
| chr5:69093971-69094113 | Common:2; Rare:35 | ||||
| chr5:69166908-69167265 | Common:3; Rare:96 | ||||
| chr5:69189453-69189611 | Common:1; Rare:48 | ||||
| chr5:69332708-69332855 | Rare:37 | ||||
| chr5:69369212-69369254 | Common:4; Rare:20 | ||||
| chr5:69369456-69369913 | Common:2; Rare:185 | ||||
| chr5:69370008-69370070 | Rare:11 | ||||
| chr5:69492284-69492586 | Common:1; Rare:74 | ||||
| chr5:69492681-69492865 | Rare:55 | ||||
| chr5:69560112-69560290 | Common:2; Rare:46 | ||||
| chr5:71587152-71587435 | Common:1; Rare:97; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:72816468-72816735 | Common:4; Rare:100 |