Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:58576641-58576982 | Common:1; Rare:124; Clinvar:1; Clinvar (benign):1 | ||||
chr1:58620290-58620575 | Common:1; Rare:47 | ||||
chr1:58783220-58783340 | Rare:33 | ||||
chr1:58785013-58785528 | Common:4; Rare:121 | ||||
chr1:58814290-58814498 | Common:1; Rare:48 | ||||
chr1:58814654-58814744 | Rare:16 | ||||
chr1:58815048-58815640 | Common:6; Rare:124 | ||||
chr1:58815832-58815916 | Common:1; Rare:7 | ||||
chr1:58816313-58816577 | Common:2; Rare:67 | ||||
chr1:58858432-58858675 | Common:3; Rare:42 | ||||
chr1:58883847-58884101 | Common:1; Rare:47 | ||||
chr1:58885385-58885625 | Common:2; Rare:34 | ||||
chr1:58899111-58899424 | Common:6; Rare:79 | ||||
chr1:58903597-58903790 | Common:1; Rare:50 | ||||
chr1:58903796-58904217 | Common:1; Rare:129 |