| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129183814-129184071 | Common:2; Rare:86 | ||||
| chr3:129249503-129249678 | Common:3; Rare:53 | ||||
| chr3:129439819-129440350 | Common:1; Rare:163; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129893585-129893882 | Rare:128 | ||||
| chr3:130893912-130894229 | Common:3; Rare:93 | ||||
| chr3:131026743-131026902 | Common:2; Rare:40 | ||||
| chr3:131381479-131381801 | Common:2; Rare:80 | ||||
| chr3:131502809-131503034 | Common:1; Rare:98 | ||||
| chr3:132659799-132659950 | Common:3; Rare:35 | ||||
| chr3:133661849-133662015 | Rare:39 | ||||
| chr3:134485407-134485766 | Rare:87 | ||||
| chr3:134485957-134486253 | Common:3; Rare:105 | ||||
| chr3:136752341-136752671 | Common:1; Rare:109 | ||||
| chr3:136819050-136819121 | Common:1; Rare:51 | ||||
| chr3:136862014-136862277 | Common:1; Rare:79 |