| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:127598223-127598458 | Common:3; Rare:68 | ||||
| chr3:127628970-127629211 | Common:1; Rare:79 | ||||
| chr3:128052179-128052504 | Common:2; Rare:111 | ||||
| chr3:128879408-128879669 | Common:4; Rare:126; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129161006-129161117 | Rare:43 | ||||
| chr3:129183794-129184079 | Common:2; Rare:95 | ||||
| chr3:129249492-129249668 | Common:3; Rare:50 | ||||
| chr3:129316283-129316289 | Rare:1 | ||||
| chr3:129439876-129440172 | Common:1; Rare:92; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:129893552-129893882 | Rare:132 | ||||
| chr3:130746796-130746934 | Common:3; Rare:40 | ||||
| chr3:131026738-131026942 | Common:2; Rare:54 | ||||
| chr3:131381479-131381801 | Common:2; Rare:80 | ||||
| chr3:131502865-131503004 | Common:1; Rare:62 | ||||
| chr3:133661772-133662008 | Rare:54 |