| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:158732150-158732560 | Common:11; Rare:151 | ||||
| chr3:158732777-158732856 | Rare:12 | ||||
| chr3:158801997-158802155 | Common:2; Rare:74 | ||||
| chr3:160399196-160399307 | Rare:30; Clinvar:1 | ||||
| chr3:160399520-160399649 | Rare:23 | ||||
| chr3:160449743-160450027 | Common:2; Rare:90 | ||||
| chr3:160565278-160565831 | Common:3; Rare:186 | ||||
| chr3:161105075-161105384 | Common:4; Rare:87 | ||||
| chr3:161221232-161221326 | Rare:29 | ||||
| chr3:167734839-167735221 | Common:3; Rare:120; Clinvar (benign):1 | ||||
| chr3:167735648-167735754 | Rare:32 | ||||
| chr3:169773258-169773429 | Rare:62 | ||||
| chr3:169812505-169812623 | Common:2; Rare:39 | ||||
| chr3:169966635-169966844 | Common:2; Rare:83 | ||||
| chr3:170870175-170870304 | Rare:63 |