| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129316242-129316289 | Rare:28 | ||||
| chr3:129439842-129440237 | Common:1; Rare:119; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:129893574-129893871 | Rare:126 | ||||
| chr3:130746796-130746947 | Common:3; Rare:44 | ||||
| chr3:131026736-131026942 | Common:2; Rare:54 | ||||
| chr3:131381464-131381801 | Common:2; Rare:85 | ||||
| chr3:131502900-131503024 | Common:1; Rare:48 | ||||
| chr3:132417213-132417544 | Common:2; Rare:100 | ||||
| chr3:133038156-133038419 | Common:1; Rare:88 | ||||
| chr3:133124597-133124824 | Rare:48 | ||||
| chr3:133661856-133662008 | Rare:35 | ||||
| chr3:134485442-134485766 | Rare:78 | ||||
| chr3:134485977-134486265 | Common:3; Rare:94 | ||||
| chr3:136196571-136196694 | Rare:38 | ||||
| chr3:136752217-136752671 | Common:2; Rare:143 |