| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48918696-48918974 | Common:2; Rare:142 | ||||
| chr3:48982835-48982909 | Rare:16 | ||||
| chr3:48982916-48983259 | Rare:67 | ||||
| chr3:48989737-48989892 | Rare:41 | ||||
| chr3:49007181-49007446 | Common:2; Rare:108 | ||||
| chr3:49018512-49018618 | Rare:46 | ||||
| chr3:49021502-49021725 | Rare:55; Clinvar:1 | ||||
| chr3:49022067-49022200 | Rare:58; Clinvar (pathogenic):1 | ||||
| chr3:49029295-49029521 | Common:2; Rare:140 | ||||
| chr3:49093580-49093648 | Rare:34 | ||||
| chr3:49104615-49104930 | Common:1; Rare:127; Clinvar:3; Clinvar (benign):7 | ||||
| chr3:49120747-49120958 | Rare:65 | ||||
| chr3:49132790-49133161 | Rare:83; Clinvar:3 | ||||
| chr3:49166289-49166437 | Common:1; Rare:38 | ||||
| chr3:49277039-49277198 | Common:1; Rare:63 |