| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128725971-128726189 | Common:1; Rare:60; Clinvar:2 | ||||
| chr3:128879421-128879676 | Common:4; Rare:125; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129161004-129161159 | Common:1; Rare:64 | ||||
| chr3:129183811-129184081 | Common:2; Rare:91 | ||||
| chr3:129249512-129249664 | Common:2; Rare:44 | ||||
| chr3:129278736-129278900 | Common:4; Rare:49 | ||||
| chr3:129316283-129316465 | Common:1; Rare:46 | ||||
| chr3:129439839-129440320 | Common:1; Rare:143; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:129893574-129893891 | Rare:133 | ||||
| chr3:130746791-130746978 | Common:3; Rare:52 | ||||
| chr3:130893933-130894263 | Common:3; Rare:99 | ||||
| chr3:131026734-131026889 | Common:2; Rare:38 | ||||
| chr3:131381518-131381801 | Common:2; Rare:67 | ||||
| chr3:131502849-131503024 | Common:1; Rare:70 | ||||
| chr3:133661869-133662011 | Rare:33 |