| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12484330-12484529 | Common:5; Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:12664074-12664315 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:13480025-13480324 | Common:2; Rare:72 | ||||
| chr3:14124691-14125150 | Common:4; Rare:133; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178564-14178863 | Common:2; Rare:157; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402437-14402621 | Rare:47 | ||||
| chr3:14651446-14651807 | Rare:104 | ||||
| chr3:14947236-14947554 | Common:4; Rare:146 | ||||
| chr3:15427447-15427629 | Common:1; Rare:62 | ||||
| chr3:15601507-15601804 | Common:4; Rare:124; Clinvar:1 | ||||
| chr3:16264874-16265229 | Common:2; Rare:115 | ||||
| chr3:16513634-16513855 | Common:4; Rare:56 | ||||
| chr3:17742534-17742952 | Common:4; Rare:151 | ||||
| chr3:19946974-19947412 | Common:5; Rare:164 | ||||
| chr3:20186139-20186541 | Common:7; Rare:122 |