Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:27370238-27370657 | Common:1; Rare:172 | ||||
chr2:27380553-27380947 | Common:2; Rare:152; Clinvar:6 | ||||
chr2:27409462-27409634 | Rare:57 | ||||
chr2:27410064-27410167 | Rare:15 | ||||
chr2:27489634-27489931 | Rare:80; Clinvar (benign):1 | ||||
chr2:27495198-27495332 | Rare:47 | ||||
chr2:27582896-27582957 | Rare:17 | ||||
chr2:27582959-27583115 | Rare:56 | ||||
chr2:27628936-27629142 | Common:1; Rare:106 | ||||
chr2:27663328-27663659 | Rare:85 | ||||
chr2:27663661-27663917 | Rare:95 | ||||
chr2:27771665-27772051 | Common:1; Rare:120 | ||||
chr2:27890364-27890836 | Common:1; Rare:127 | ||||
chr2:28751495-28752142 | Common:4; Rare:259 | ||||
chr2:28870221-28870475 | Rare:115 |