| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140401395-140401912 | Common:3; Rare:118 | ||||
| chr5:140547441-140547746 | Common:2; Rare:69 | ||||
| chr5:140557389-140557519 | Common:1; Rare:83 | ||||
| chr5:140564296-140564470 | Common:1; Rare:49 | ||||
| chr5:140564479-140564590 | Rare:18 | ||||
| chr5:140564594-140564845 | Rare:70 | ||||
| chr5:140633529-140633808 | Common:5; Rare:59 | ||||
| chr5:140647562-140647923 | Common:5; Rare:147; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140664733-140665063 | Common:4; Rare:105 | ||||
| chr5:140691309-140691677 | Common:1; Rare:130; Clinvar:10; Clinvar (benign):2 | ||||
| chr5:141320725-141320920 | Common:2; Rare:69 | ||||
| chr5:141421026-141421096 | Common:1; Rare:17 | ||||
| chr5:141636810-141637012 | Common:2; Rare:87 | ||||
| chr5:141637368-141637487 | Rare:25 | ||||
| chr5:141682191-141682328 | Common:1; Rare:45 |