| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:56435467-56435973 | Common:6; Rare:166 | ||||
| chr4:56435994-56436320 | Rare:116 | ||||
| chr4:56467519-56467704 | Common:2; Rare:76; Clinvar (benign):5 | ||||
| chr4:56977559-56977785 | Common:2; Rare:86 | ||||
| chr4:57110382-57110569 | Common:2; Rare:57 | ||||
| chr4:65669476-65669606 | Common:1; Rare:33 | ||||
| chr4:65670285-65670636 | Common:2; Rare:94 | ||||
| chr4:67545351-67545748 | Common:2; Rare:99 | ||||
| chr4:67701115-67701409 | Common:4; Rare:138 | ||||
| chr4:68349945-68350206 | Rare:95 | ||||
| chr4:69051271-69051454 | Common:3; Rare:38 | ||||
| chr4:70050191-70050486 | Common:3; Rare:61 | ||||
| chr4:70688451-70688623 | Common:2; Rare:51 | ||||
| chr4:70734276-70734469 | Rare:31 | ||||
| chr4:70902127-70902503 | Common:6; Rare:129 |