| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:32165659-32165903 | Common:1; Rare:97 | ||||
| chr2:32277747-32278019 | Common:2; Rare:65 | ||||
| chr2:32627924-32628139 | Rare:65 | ||||
| chr2:33457995-33458109 | Common:1; Rare:20 | ||||
| chr2:33476269-33476482 | Common:3; Rare:47 | ||||
| chr2:33476595-33476691 | Rare:18 | ||||
| chr2:33599222-33599455 | Common:1; Rare:85 | ||||
| chr2:37084262-37084561 | Common:4; Rare:111 | ||||
| chr2:37196428-37196516 | Rare:26 | ||||
| chr2:37231542-37231743 | Common:4; Rare:119; Clinvar:1; Clinvar (benign):4 | ||||
| chr2:37324698-37324918 | Common:1; Rare:85 | ||||
| chr2:37671486-37671736 | Common:1; Rare:96 | ||||
| chr2:37925460-37925575 | Common:1; Rare:51 | ||||
| chr2:38602599-38602758 | Rare:51 | ||||
| chr2:38602876-38603187 | Common:4; Rare:124 |