| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:158732165-158732247 | Common:2; Rare:27 | ||||
| chr3:158732694-158732945 | Common:1; Rare:41 | ||||
| chr3:158801960-158802161 | Common:2; Rare:92 | ||||
| chr3:159763606-159764176 | Common:2; Rare:187 | ||||
| chr3:159764314-159764535 | Common:1; Rare:64 | ||||
| chr3:160399184-160399697 | Rare:144; Clinvar:7 | ||||
| chr3:160565284-160565843 | Common:3; Rare:188 | ||||
| chr3:160755449-160755664 | Common:1; Rare:82 | ||||
| chr3:160755922-160756254 | Common:1; Rare:86 | ||||
| chr3:160756287-160756553 | Rare:70 | ||||
| chr3:161105254-161105383 | Common:2; Rare:44 | ||||
| chr3:167734816-167735071 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735602-167735752 | Rare:39 | ||||
| chr3:168095874-168096071 | Rare:65 | ||||
| chr3:169769390-169769429 | Rare:21 |