Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:205750171-205750394 | Common:2; Rare:51 | ||||
chr1:206612420-206612648 | Common:3; Rare:66 | ||||
chr1:207050957-207051096 | Common:1; Rare:62 | ||||
chr1:207052969-207053300 | Common:1; Rare:86 | ||||
chr1:207321755-207321848 | Rare:25 | ||||
chr1:207322126-207322475 | Rare:108 | ||||
chr1:207751920-207752178 | Common:1; Rare:80 | ||||
chr1:207911080-207911227 | Common:1; Rare:42 | ||||
chr1:208244255-208244540 | Common:1; Rare:84 | ||||
chr1:209675083-209675557 | Common:4; Rare:121 | ||||
chr1:209784526-209784704 | Rare:57 | ||||
chr1:209827838-209828083 | Common:1; Rare:66 | ||||
chr1:209937944-209938273 | Common:3; Rare:116; Clinvar (pathogenic):1 | ||||
chr1:210328815-210328922 | Common:1; Rare:39 | ||||
chr1:211259077-211259417 | Common:1; Rare:109 |