| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128650537-128650663 | Rare:86 | ||||
| chr3:128650736-128650984 | Common:4; Rare:185 | ||||
| chr3:128680683-128680939 | Common:4; Rare:155 | ||||
| chr3:128680980-128681360 | Common:2; Rare:185 | ||||
| chr3:128726050-128726270 | Common:2; Rare:128; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:128879346-128879795 | Common:9; Rare:360; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr3:129161013-129161477 | Common:3; Rare:178 | ||||
| chr3:129183672-129184129 | Common:6; Rare:292 | ||||
| chr3:129249453-129249724 | Common:6; Rare:147 | ||||
| chr3:129278713-129279051 | Common:8; Rare:177 | ||||
| chr3:129315673-129315920 | Common:6; Rare:150 | ||||
| chr3:129316065-129316377 | Common:4; Rare:200 | ||||
| chr3:129316620-129316930 | Common:7; Rare:96 | ||||
| chr3:129439758-129440439 | Common:6; Rare:306; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:129606643-129606928 | Common:8; Rare:123 |