| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14124719-14125087 | Common:4; Rare:109; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178566-14178878 | Common:2; Rare:161; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14651651-14651793 | Rare:43 | ||||
| chr3:14947412-14947563 | Common:2; Rare:74 | ||||
| chr3:15206047-15206269 | Rare:83 | ||||
| chr3:15427478-15427641 | Common:1; Rare:56 | ||||
| chr3:15601519-15601746 | Common:4; Rare:91 | ||||
| chr3:16264922-16265229 | Common:2; Rare:84 | ||||
| chr3:20186176-20186423 | Common:2; Rare:80 | ||||
| chr3:21751097-21751415 | Common:4; Rare:103 | ||||
| chr3:23916922-23917177 | Rare:95 | ||||
| chr3:25790047-25790118 | Common:2; Rare:29 | ||||
| chr3:28348807-28349175 | Common:3; Rare:114 | ||||
| chr3:29280962-29281076 | Common:2; Rare:17 | ||||
| chr3:31981634-31981826 | Common:1; Rare:48 |