| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196712578-196712697 | Rare:40 | ||||
| chr3:196867758-196867953 | Rare:69 | ||||
| chr3:196942394-196942716 | Common:1; Rare:139 | ||||
| chr3:197029780-197029938 | Common:1; Rare:51 | ||||
| chr3:197736833-197737214 | Common:3; Rare:126 | ||||
| chr3:197791111-197791281 | Common:2; Rare:58 | ||||
| chr3:197949885-197950283 | Common:4; Rare:118; Clinvar (benign):2 | ||||
| chr3:197950633-197950978 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:197959958-197960255 | Common:1; Rare:105 | ||||
| chr4:53094-53377 | Rare:5 | ||||
| chr4:124302-124530 | Common:6; Rare:58 | ||||
| chr4:305443-305615 | Common:2; Rare:55 | ||||
| chr4:337421-337873 | Common:3; Rare:131 | ||||
| chr4:499123-499313 | Common:3; Rare:77 | ||||
| chr4:663565-663807 | Common:1; Rare:98; Clinvar:1 |