| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128725849-128726253 | Common:1; Rare:114; Clinvar:3 | ||||
| chr3:128879404-128879694 | Common:4; Rare:144; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:129001232-129001328 | Common:1; Rare:25 | ||||
| chr3:129160991-129161153 | Common:1; Rare:65 | ||||
| chr3:129183685-129184119 | Common:4; Rare:160 | ||||
| chr3:129249534-129249686 | Common:1; Rare:46 | ||||
| chr3:129278761-129279002 | Common:4; Rare:69 | ||||
| chr3:129316242-129316366 | Common:1; Rare:52 | ||||
| chr3:129316663-129316786 | Common:1; Rare:25 | ||||
| chr3:129439819-129440382 | Common:1; Rare:169; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129562909-129563096 | Common:3; Rare:58 | ||||
| chr3:129893514-129893882 | Rare:139 | ||||
| chr3:130746771-130746929 | Common:3; Rare:52 | ||||
| chr3:130893894-130894294 | Common:3; Rare:116 | ||||
| chr3:131026729-131026968 | Common:2; Rare:62 |