| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:36355450-36356084 | Common:4; Rare:214 | ||||
| chr2:36356234-36356618 | Common:2; Rare:154 | ||||
| chr2:36551774-36552005 | Common:2; Rare:63 | ||||
| chr2:36581288-36581567 | Rare:91 | ||||
| chr2:36597875-36598075 | Common:5; Rare:88 | ||||
| chr2:37084275-37084561 | Common:3; Rare:108 | ||||
| chr2:37196403-37196531 | Rare:49 | ||||
| chr2:37231413-37231764 | Common:6; Rare:177; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:37324693-37324909 | Common:1; Rare:82 | ||||
| chr2:37671428-37671970 | Common:12; Rare:171 | ||||
| chr2:37925154-37925406 | Common:3; Rare:103 | ||||
| chr2:38300581-38300648 | Rare:9 | ||||
| chr2:38377239-38377487 | Common:2; Rare:103 | ||||
| chr2:38746689-38746789 | Rare:33 | ||||
| chr2:38747071-38747285 | Common:1; Rare:67 |