| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42591046-42591993 | Common:12; Rare:518 | ||||
| chr3:42600234-42601040 | Common:20; Rare:1472 | ||||
| chr3:42601040-42601888 | Common:5; Rare:653 | ||||
| chr3:42654060-42654660 | Common:5; Rare:323 | ||||
| chr3:42773059-42773459 | Common:5; Rare:198 | ||||
| chr3:42803728-42804160 | Common:3; Rare:239 | ||||
| chr3:42804180-42804761 | Common:13; Rare:619 | ||||
| chr3:42804915-42805558 | Common:2; Rare:96 | ||||
| chr3:42856020-42856350 | Common:2; Rare:53 | ||||
| chr3:42936146-42936546 | Common:5; Rare:157 | ||||
| chr3:43105320-43105720 | Common:4; Rare:126 | ||||
| chr3:43105860-43106420 | Common:12; Rare:363 | ||||
| chr3:43286300-43286700 | Common:9; Rare:496 | ||||
| chr3:43621868-43622464 | Common:14; Rare:899; Clinvar:48; Clinvar (benign):7 | ||||
| chr3:43638644-43638953 | Common:1; Rare:103 |