| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:158110029-158110202 | Rare:42 | ||||
| chr3:158672459-158672726 | Common:2; Rare:75 | ||||
| chr3:158672729-158672916 | Common:2; Rare:32 | ||||
| chr3:158732139-158732389 | Common:9; Rare:76 | ||||
| chr3:158732735-158732923 | Rare:29 | ||||
| chr3:158801984-158802168 | Common:2; Rare:86 | ||||
| chr3:160399171-160399406 | Rare:66; Clinvar:4 | ||||
| chr3:160399512-160399669 | Rare:34 | ||||
| chr3:160565278-160565845 | Common:3; Rare:191 | ||||
| chr3:161105284-161105602 | Common:3; Rare:89 | ||||
| chr3:161221178-161221371 | Common:2; Rare:65 | ||||
| chr3:167734807-167735229 | Common:3; Rare:140; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735564-167735731 | Rare:40 | ||||
| chr3:169663379-169663728 | Common:2; Rare:87 | ||||
| chr3:169772693-169772802 | Common:1; Rare:27 |