| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129183814-129184079 | Common:2; Rare:89 | ||||
| chr3:129249492-129249675 | Common:3; Rare:55 | ||||
| chr3:129278736-129278888 | Common:4; Rare:48 | ||||
| chr3:129316268-129316317 | Rare:26 | ||||
| chr3:129439838-129440234 | Common:1; Rare:119; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:129893545-129893882 | Rare:132 | ||||
| chr3:130746771-130746979 | Common:3; Rare:64 | ||||
| chr3:130893919-130894242 | Common:3; Rare:93 | ||||
| chr3:131026729-131026951 | Common:2; Rare:55 | ||||
| chr3:131381464-131381832 | Common:2; Rare:101 | ||||
| chr3:131502809-131502995 | Common:1; Rare:89 | ||||
| chr3:132417203-132417662 | Common:3; Rare:151 | ||||
| chr3:132597183-132597275 | Common:1; Rare:14 | ||||
| chr3:132659799-132659937 | Common:3; Rare:31 | ||||
| chr3:132722132-132722248 | Common:1; Rare:51; Clinvar:6; Clinvar (benign):2 |