| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:65624947-65625058 | Common:1; Rare:37 | ||||
| chr5:65721971-65722263 | Common:2; Rare:98 | ||||
| chr5:65926401-65926719 | Common:5; Rare:98 | ||||
| chr5:66144416-66144535 | Rare:30 | ||||
| chr5:69166906-69167168 | Common:2; Rare:62 | ||||
| chr5:69189428-69189759 | Common:1; Rare:104 | ||||
| chr5:69217617-69217897 | Common:4; Rare:93 | ||||
| chr5:69332742-69332855 | Rare:32 | ||||
| chr5:69369187-69369358 | Common:4; Rare:47 | ||||
| chr5:69369461-69369933 | Common:2; Rare:185 | ||||
| chr5:69370016-69370213 | Rare:37 | ||||
| chr5:69560032-69560290 | Common:3; Rare:68 | ||||
| chr5:71455500-71455657 | Rare:43 | ||||
| chr5:71587158-71587404 | Common:1; Rare:80; Clinvar (benign):1 | ||||
| chr5:72106982-72107711 | Common:3; Rare:238 |