| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129439844-129440168 | Common:1; Rare:100; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:129893580-129893875 | Rare:127 | ||||
| chr3:130746796-130746913 | Common:3; Rare:37 | ||||
| chr3:131026734-131026942 | Common:2; Rare:54 | ||||
| chr3:131381609-131381801 | Common:2; Rare:45 | ||||
| chr3:132596964-132597310 | Common:1; Rare:43 | ||||
| chr3:132659799-132659914 | Common:3; Rare:24 | ||||
| chr3:132722102-132722255 | Common:1; Rare:64; Clinvar:9; Clinvar (benign):2 | ||||
| chr3:133661789-133662033 | Rare:58 | ||||
| chr3:134485437-134485766 | Rare:79 | ||||
| chr3:134485977-134486202 | Common:2; Rare:71 | ||||
| chr3:136752341-136752710 | Common:1; Rare:121 | ||||
| chr3:136862031-136862275 | Common:1; Rare:68 | ||||
| chr3:138115594-138115694 | Common:3; Rare:23 | ||||
| chr3:138594202-138594451 | Rare:74 |