| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129120643-129120835 | Common:1; Rare:42 | ||||
| chr3:129561672-129561923 | Common:2; Rare:85 | ||||
| chr3:130111461-130111753 | Common:3; Rare:72 | ||||
| chr3:131361598-131361931 | Common:3; Rare:101 | ||||
| chr3:133541184-133541323 | Rare:23 | ||||
| chr3:136625236-136625398 | Rare:34 | ||||
| chr3:139352510-139352783 | Rare:73; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:139354607-139354656 | Common:1; Rare:5 | ||||
| chr3:139357890-139358145 | Common:2; Rare:58 | ||||
| chr3:139362433-139362735 | Common:2; Rare:67 | ||||
| chr3:142941447-142941620 | Common:1; Rare:26 | ||||
| chr3:142941688-142941748 | Rare:10 | ||||
| chr3:149173996-149174245 | Common:3; Rare:37 | ||||
| chr3:149174795-149175036 | Rare:40 | ||||
| chr3:149205997-149206341 | Common:2; Rare:95; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 |