| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:36521922-36522308 | Common:1; Rare:99 | ||||
| chr2:36532648-36532651 | |||||
| chr2:36533611-36533934 | Rare:83 | ||||
| chr2:36536256-36536527 | Common:2; Rare:54 | ||||
| chr2:36540322-36540480 | Rare:29 | ||||
| chr2:36544313-36544434 | Common:1; Rare:38 | ||||
| chr2:37599766-37599911 | Common:3; Rare:33 | ||||
| chr2:37920702-37920926 | Common:3; Rare:46 | ||||
| chr2:38995262-38995515 | Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:42057086-42057394 | Rare:84 | ||||
| chr2:42170334-42170465 | Common:1; Rare:31 | ||||
| chr2:42286996-42287159 | Common:1; Rare:33 | ||||
| chr2:42810425-42810536 | Common:1; Rare:55 | ||||
| chr2:46256714-46256868 | Rare:29 | ||||
| chr2:46298836-46298937 | Rare:21 |