| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128488464-128488719 | Common:2; Rare:100 | ||||
| chr3:128488844-128489272 | Common:1; Rare:86 | ||||
| chr3:128650070-128650818 | Common:9; Rare:353 | ||||
| chr3:128680560-128680950 | Common:6; Rare:215 | ||||
| chr3:128680960-128681590 | Common:3; Rare:256 | ||||
| chr3:128879394-128879707 | Common:8; Rare:289; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr3:129121765-129121973 | Common:1; Rare:33 | ||||
| chr3:129122020-129122390 | Common:3; Rare:92 | ||||
| chr3:129160991-129161152 | Common:1; Rare:107 | ||||
| chr3:129161230-129161520 | Common:6; Rare:164 | ||||
| chr3:129183771-129184113 | Common:4; Rare:236 | ||||
| chr3:129249481-129249715 | Common:5; Rare:130 | ||||
| chr3:129278764-129279042 | Common:6; Rare:148 | ||||
| chr3:129316089-129316360 | Common:3; Rare:123 | ||||
| chr3:129316282-129316384 | Common:1; Rare:29 |