| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129893585-129893882 | Rare:128 | ||||
| chr3:130746796-130746934 | Common:3; Rare:40 | ||||
| chr3:130893905-130894252 | Common:3; Rare:100 | ||||
| chr3:131026725-131026889 | Common:2; Rare:39 | ||||
| chr3:131381464-131381801 | Common:2; Rare:85 | ||||
| chr3:132417328-132417654 | Common:3; Rare:107 | ||||
| chr3:132659799-132659937 | Common:3; Rare:31 | ||||
| chr3:133661856-133662033 | Rare:41 | ||||
| chr3:134485356-134485772 | Rare:95 | ||||
| chr3:134485957-134486242 | Common:3; Rare:100 | ||||
| chr3:135965534-135965771 | Common:1; Rare:106 | ||||
| chr3:136250318-136250412 | Common:2; Rare:51; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr3:136752360-136752671 | Common:1; Rare:108 | ||||
| chr3:136818977-136819177 | Common:4; Rare:103 | ||||
| chr3:136862022-136862282 | Common:1; Rare:76 |