| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:182793334-182793617 | Common:3; Rare:79 | ||||
| chr3:183099443-183099742 | Common:2; Rare:96; Clinvar:3; Clinvar (benign):5 | ||||
| chr3:184017862-184018080 | Common:1; Rare:66 | ||||
| chr3:184135215-184135398 | Common:2; Rare:55; Clinvar:5 | ||||
| chr3:184185861-184186210 | Common:5; Rare:131 | ||||
| chr3:184248868-184249032 | Common:1; Rare:86; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:184249489-184249794 | Common:1; Rare:96 | ||||
| chr3:184298968-184299279 | Common:2; Rare:91 | ||||
| chr3:184305571-184305929 | Common:2; Rare:74 | ||||
| chr3:184306471-184306622 | Rare:42 | ||||
| chr3:184314435-184314671 | Common:3; Rare:68 | ||||
| chr3:184320058-184320309 | Rare:44 | ||||
| chr3:184335866-184335956 | Rare:30 | ||||
| chr3:184361601-184361765 | Rare:43 | ||||
| chr3:184362157-184362276 | Common:1; Rare:18 |