| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:186628151-186628732 | Common:4; Rare:190; Clinvar:1 | ||||
| chr4:186635578-186635860 | Common:1; Rare:51 | ||||
| chr4:186719383-186719503 | Rare:30 | ||||
| chr4:186727259-186727464 | Rare:32 | ||||
| chr4:187307133-187307489 | Common:3; Rare:67 | ||||
| chr4:187319986-187320129 | Rare:23 | ||||
| chr4:187523940-187524144 | Common:3; Rare:37 | ||||
| chr4:188017837-188018024 | Common:1; Rare:33 | ||||
| chr4:188107947-188108163 | Common:1; Rare:41 | ||||
| chr4:189473596-189473795 | Common:2; Rare:27 | ||||
| chr5:473841-474077 | Common:3; Rare:49 | ||||
| chr5:474130-474402 | Common:6; Rare:14 | ||||
| chr5:784728-784901 | Common:4; Rare:57 | ||||
| chr5:906594-906686 | Rare:16 | ||||
| chr5:1328760-1328852 | Common:3; Rare:12 |