| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128879401-128879663 | Common:4; Rare:123; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129161013-129161169 | Common:1; Rare:61 | ||||
| chr3:129183814-129184071 | Common:2; Rare:86 | ||||
| chr3:129278673-129278892 | Common:4; Rare:66 | ||||
| chr3:129439916-129440320 | Common:1; Rare:119; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:130893905-130894207 | Common:2; Rare:91 | ||||
| chr3:131026772-131026902 | Common:2; Rare:28 | ||||
| chr3:131502829-131503004 | Common:1; Rare:80 | ||||
| chr3:134485973-134486185 | Common:2; Rare:66 | ||||
| chr3:136862032-136862269 | Common:1; Rare:64 | ||||
| chr3:138594209-138594451 | Rare:70 | ||||
| chr3:139389608-139389868 | Common:1; Rare:80 | ||||
| chr3:141486874-141487074 | Common:1; Rare:62 | ||||
| chr3:142447985-142448145 | Common:1; Rare:59 | ||||
| chr3:143001473-143001634 | Common:2; Rare:56 |