| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128123772-128124018 | Rare:61 | ||||
| chr3:128153365-128153505 | Rare:41 | ||||
| chr3:128650605-128650663 | Rare:22 | ||||
| chr3:128879408-128879694 | Common:4; Rare:141; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:129001194-129001330 | Common:1; Rare:35 | ||||
| chr3:129161013-129161133 | Rare:48 | ||||
| chr3:129183784-129184045 | Common:2; Rare:84 | ||||
| chr3:129249509-129249683 | Common:3; Rare:53 | ||||
| chr3:129278594-129278882 | Common:5; Rare:78 | ||||
| chr3:129316270-129316350 | Rare:31 | ||||
| chr3:129439829-129440350 | Common:1; Rare:161; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129893545-129893881 | Rare:131 | ||||
| chr3:130893905-130894244 | Common:3; Rare:99 | ||||
| chr3:131026720-131026940 | Common:2; Rare:56 | ||||
| chr3:131381092-131381256 | Rare:32 |