| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129249545-129249693 | Common:1; Rare:45 | ||||
| chr3:129278754-129278882 | Common:4; Rare:42 | ||||
| chr3:129439876-129440350 | Common:1; Rare:146; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129893585-129893882 | Rare:128 | ||||
| chr3:130893917-130894205 | Common:2; Rare:86 | ||||
| chr3:131026772-131026909 | Common:2; Rare:30 | ||||
| chr3:131381531-131381797 | Common:2; Rare:61 | ||||
| chr3:131502782-131503016 | Common:1; Rare:97 | ||||
| chr3:133661837-133662021 | Rare:42 | ||||
| chr3:134374440-134374705 | Common:1; Rare:81 | ||||
| chr3:134485461-134485772 | Rare:77 | ||||
| chr3:134485977-134486181 | Common:2; Rare:61 | ||||
| chr3:136862032-136862277 | Common:1; Rare:68 | ||||
| chr3:138174855-138174958 | Common:1; Rare:21 | ||||
| chr3:139389568-139389851 | Common:1; Rare:93 |