| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:132673602-132673630 | Rare:8 | ||||
| chr3:134328271-134328493 | Rare:49 | ||||
| chr3:134464056-134464328 | Common:1; Rare:49 | ||||
| chr3:136332575-136332860 | Common:1; Rare:63 | ||||
| chr3:136737253-136737425 | Common:1; Rare:30 | ||||
| chr3:136851707-136851757 | Rare:9 | ||||
| chr3:136942808-136943100 | Common:1; Rare:53 | ||||
| chr3:138051053-138051159 | Common:2; Rare:18 | ||||
| chr3:139354550-139354663 | Common:2; Rare:16 | ||||
| chr3:139373301-139373850 | Rare:98; Clinvar (pathogenic):1 | ||||
| chr3:141897177-141897299 | Common:1; Rare:18 | ||||
| chr3:141908784-141908948 | Common:1; Rare:30 | ||||
| chr3:149966855-149967055 | Common:1; Rare:34 | ||||
| chr3:150408860-150409005 | Rare:43 | ||||
| chr3:150430423-150430456 | Rare:8 |