| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:46539234-46539391 | Common:1; Rare:37 | ||||
| chr3:46541914-46542110 | Common:1; Rare:31 | ||||
| chr3:46547045-46547202 | Rare:19 | ||||
| chr3:46558405-46558655 | Common:3; Rare:52 | ||||
| chr3:46845867-46846147 | Common:3; Rare:63 | ||||
| chr3:46926981-46927060 | Rare:17 | ||||
| chr3:46927273-46927598 | Rare:59 | ||||
| chr3:46930146-46930318 | Rare:29 | ||||
| chr3:46943670-46943803 | Common:1; Rare:16 | ||||
| chr3:46955909-46956214 | Rare:56 | ||||
| chr3:46980658-46980762 | Rare:16 | ||||
| chr3:46987716-46988049 | Common:2; Rare:105 | ||||
| chr3:47009245-47009617 | Common:5; Rare:148; Clinvar:5; Clinvar (benign):4 | ||||
| chr3:47164715-47164865 | Common:3; Rare:32 | ||||
| chr3:47175784-47176130 | Common:1; Rare:46 |