| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:43229252-43229349 | Common:1; Rare:18 | ||||
| chr2:46556270-46556459 | Rare:38 | ||||
| chr2:46587448-46587707 | Common:3; Rare:48 | ||||
| chr2:46590054-46590342 | Rare:45 | ||||
| chr2:46699834-46700060 | Common:1; Rare:53 | ||||
| chr2:46850854-46851039 | Rare:43 | ||||
| chr2:47043689-47043919 | Rare:56 | ||||
| chr2:47171196-47171417 | Common:1; Rare:50 | ||||
| chr2:47174922-47175220 | Common:6; Rare:84 | ||||
| chr2:47802577-47802601 | Rare:7 | ||||
| chr2:47803316-47803461 | Common:1; Rare:59; Clinvar:12; Clinvar (benign):13 | ||||
| chr2:47818778-47818958 | Common:2; Rare:37 | ||||
| chr2:47906467-47906818 | Common:2; Rare:129 | ||||
| chr2:53801399-53801839 | Rare:108 | ||||
| chr2:54457917-54458027 | Rare:33 |