| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:157436810-157436866 | Rare:10 | ||||
| chr3:158644507-158644659 | Common:5; Rare:59; Clinvar (benign):6 | ||||
| chr3:158660046-158660269 | Common:2; Rare:23 | ||||
| chr3:158672423-158672731 | Common:3; Rare:90 | ||||
| chr3:158801984-158802155 | Common:2; Rare:80 | ||||
| chr3:159763170-159763315 | Rare:27 | ||||
| chr3:159764331-159764476 | Common:1; Rare:35 | ||||
| chr3:159839827-159840158 | Common:2; Rare:72 | ||||
| chr3:159852649-159852973 | Rare:52 | ||||
| chr3:159853005-159853184 | Rare:30 | ||||
| chr3:159853205-159853295 | Rare:18 | ||||
| chr3:160399196-160399307 | Rare:30; Clinvar:1 | ||||
| chr3:160399518-160399669 | Rare:31 | ||||
| chr3:160565330-160565837 | Common:3; Rare:173 | ||||
| chr3:161221159-161221369 | Common:2; Rare:70 |