| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49007579-49008080 | Common:2; Rare:191 | ||||
| chr3:49017806-49018260 | Rare:294 | ||||
| chr3:49018297-49018468 | Common:2; Rare:98 | ||||
| chr3:49018444-49018743 | Common:2; Rare:232 | ||||
| chr3:49019820-49020598 | Common:3; Rare:256 | ||||
| chr3:49020651-49020848 | Common:2; Rare:92 | ||||
| chr3:49021218-49021898 | Common:3; Rare:354; Clinvar:10; Clinvar (benign):3 | ||||
| chr3:49021883-49022361 | Rare:329; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr3:49027695-49027869 | Rare:55 | ||||
| chr3:49029298-49029573 | Common:3; Rare:249 | ||||
| chr3:49093374-49093486 | Rare:22 | ||||
| chr3:49093580-49093684 | Common:1; Rare:47 | ||||
| chr3:49093921-49094197 | Rare:166 | ||||
| chr3:49094289-49094464 | Common:1; Rare:74 | ||||
| chr3:49104380-49104650 | Rare:150; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):2 |