| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:158672550-158672721 | Common:2; Rare:48 | ||||
| chr3:158732159-158732221 | Common:2; Rare:17 | ||||
| chr3:158732245-158732318 | Common:3; Rare:18 | ||||
| chr3:158801976-158802161 | Common:2; Rare:84 | ||||
| chr3:159763596-159763746 | Rare:44 | ||||
| chr3:159764331-159764458 | Common:1; Rare:35 | ||||
| chr3:160399164-160399669 | Rare:138; Clinvar:7 | ||||
| chr3:160400356-160400385 | Rare:6 | ||||
| chr3:160565271-160565360 | Common:1; Rare:24 | ||||
| chr3:160565406-160565842 | Common:2; Rare:155 | ||||
| chr3:160676989-160677238 | Common:3; Rare:33 | ||||
| chr3:160755442-160755664 | Common:1; Rare:83 | ||||
| chr3:167734799-167735245 | Common:4; Rare:147; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735615-167735706 | Rare:18 | ||||
| chr3:168094781-168095039 | Common:2; Rare:46 |