| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:65563124-65563326 | Common:3; Rare:75 | ||||
| chr5:65624950-65625073 | Common:1; Rare:42 | ||||
| chr5:65925533-65925996 | Rare:173 | ||||
| chr5:65926544-65926722 | Common:5; Rare:50 | ||||
| chr5:66144154-66144351 | Common:2; Rare:69 | ||||
| chr5:67004055-67004291 | Common:3; Rare:85 | ||||
| chr5:68215502-68215828 | Common:4; Rare:116 | ||||
| chr5:68216241-68216262 | Common:1; Rare:6 | ||||
| chr5:68280767-68280979 | Rare:40; Clinvar (benign):1 | ||||
| chr5:68288305-68288742 | Common:4; Rare:139 | ||||
| chr5:68290530-68290761 | Rare:52; Clinvar:1 | ||||
| chr5:68292503-68292626 | Rare:30 | ||||
| chr5:69166919-69167160 | Common:2; Rare:55 | ||||
| chr5:69189484-69189590 | Common:1; Rare:33 | ||||
| chr5:69332701-69332855 | Rare:37 |