Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:207050950-207051083 | Common:1; Rare:62 | ||||
chr1:207052935-207053300 | Common:1; Rare:95 | ||||
chr1:207321724-207321788 | Rare:19 | ||||
chr1:207751915-207752284 | Common:2; Rare:120; Clinvar:1 | ||||
chr1:208243852-208243943 | Rare:23 | ||||
chr1:208243993-208244102 | Rare:18 | ||||
chr1:208244186-208244553 | Common:2; Rare:97 | ||||
chr1:208244747-208244880 | Rare:27 | ||||
chr1:209675253-209675431 | Common:2; Rare:44 | ||||
chr1:209784499-209784704 | Rare:68 | ||||
chr1:209827842-209828064 | Common:1; Rare:59 | ||||
chr1:209937960-209938274 | Common:3; Rare:107; Clinvar (pathogenic):1 | ||||
chr1:210232469-210232653 | Common:1; Rare:32 | ||||
chr1:210232800-210232960 | Common:1; Rare:46 | ||||
chr1:210237105-210237431 | Common:1; Rare:56 |