Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:225810291-225810442 | Common:2; Rare:30 | ||||
chr1:225881719-225881919 | Common:3; Rare:43 | ||||
chr1:225882228-225882563 | Common:3; Rare:85 | ||||
chr1:225882847-225883035 | Common:3; Rare:49 | ||||
chr1:225923534-225923783 | Common:1; Rare:70; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:225924039-225924549 | Common:11; Rare:169 | ||||
chr1:225924661-225924749 | Rare:14 | ||||
chr1:225999256-225999671 | Common:2; Rare:165 | ||||
chr1:226061806-226061878 | Rare:17 | ||||
chr1:226061896-226061988 | Rare:23 | ||||
chr1:226062021-226062307 | Common:1; Rare:99 | ||||
chr1:226062385-226062869 | Common:1; Rare:168 | ||||
chr1:226062989-226063188 | Rare:63 | ||||
chr1:226063228-226063561 | Common:2; Rare:94 | ||||
chr1:226063674-226063725 | Common:1; Rare:11 |