| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15601812-15602059 | Common:2; Rare:123; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:15859511-15859680 | Common:3; Rare:44 | ||||
| chr3:15859772-15860230 | Common:5; Rare:137 | ||||
| chr3:16264874-16265244 | Common:2; Rare:122 | ||||
| chr3:16513481-16513775 | Common:4; Rare:76 | ||||
| chr3:16513912-16513927 | Rare:3 | ||||
| chr3:16513980-16514032 | Rare:3 | ||||
| chr3:16884475-16884781 | Common:3; Rare:60 | ||||
| chr3:16884983-16885364 | Common:8; Rare:104 | ||||
| chr3:16885424-16885586 | Rare:34 | ||||
| chr3:17742513-17742927 | Common:3; Rare:144 | ||||
| chr3:19148153-19148608 | Common:3; Rare:113 | ||||
| chr3:19946951-19947457 | Common:7; Rare:188 | ||||
| chr3:20040487-20040645 | Rare:54 | ||||
| chr3:20186176-20186418 | Common:2; Rare:77 |