| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:180036754-180036799 | Rare:12 | ||||
| chr3:180036922-180037176 | Rare:64 | ||||
| chr3:180601985-180602209 | Common:1; Rare:63 | ||||
| chr3:180679467-180679568 | Rare:20; Clinvar:2 | ||||
| chr3:180912336-180912713 | Common:4; Rare:124 | ||||
| chr3:180989606-180989782 | Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:181711736-181711996 | Rare:78 | ||||
| chr3:181712278-181712609 | Common:1; Rare:86; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr3:183099437-183099742 | Common:2; Rare:100; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr3:183635475-183635670 | Common:2; Rare:61 | ||||
| chr3:183697673-183697904 | Common:2; Rare:105 | ||||
| chr3:183698030-183698192 | Rare:54 | ||||
| chr3:184017868-184018103 | Common:1; Rare:73 | ||||
| chr3:184135221-184135413 | Common:2; Rare:60; Clinvar:5 | ||||
| chr3:184185856-184186210 | Common:5; Rare:133 |