| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128725952-128726210 | Common:1; Rare:67; Clinvar:2 | ||||
| chr3:128879404-128879694 | Common:4; Rare:144; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:128994068-128994229 | Common:1; Rare:54 | ||||
| chr3:129161340-129161435 | Common:1; Rare:29 | ||||
| chr3:129183814-129184114 | Common:2; Rare:113 | ||||
| chr3:129249498-129249715 | Common:3; Rare:65 | ||||
| chr3:129278777-129278920 | Common:3; Rare:40 | ||||
| chr3:129316242-129316340 | Rare:48 | ||||
| chr3:129439847-129440382 | Common:1; Rare:161; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129893523-129893882 | Rare:137 | ||||
| chr3:129974453-129974820 | Common:4; Rare:87 | ||||
| chr3:130746792-130746947 | Common:3; Rare:45 | ||||
| chr3:130893919-130894258 | Common:3; Rare:98 | ||||
| chr3:131026710-131026951 | Common:2; Rare:58 | ||||
| chr3:131381451-131381832 | Common:3; Rare:103 |