| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129249524-129249739 | Common:2; Rare:61 | ||||
| chr3:129278683-129278890 | Common:4; Rare:64 | ||||
| chr3:129316270-129316317 | Rare:25 | ||||
| chr3:129439805-129440350 | Common:1; Rare:168; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129688309-129688377 | Rare:10 | ||||
| chr3:129893580-129893875 | Rare:127 | ||||
| chr3:131026725-131026942 | Common:2; Rare:55 | ||||
| chr3:131381464-131381811 | Common:2; Rare:89 | ||||
| chr3:131502839-131503016 | Common:1; Rare:75 | ||||
| chr3:132659783-132659928 | Common:3; Rare:32 | ||||
| chr3:133661856-133662010 | Rare:35 | ||||
| chr3:134374417-134374659 | Common:1; Rare:71 | ||||
| chr3:134485402-134485766 | Rare:87 | ||||
| chr3:134485945-134486265 | Common:4; Rare:112 | ||||
| chr3:136196298-136196439 | Rare:54 |