Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:64848109-64848199 | Rare:15 | ||||
chr1:64966339-64966652 | Common:1; Rare:108 | ||||
chr1:65147479-65147653 | Rare:56 | ||||
chr1:65148086-65148315 | Common:3; Rare:47 | ||||
chr1:65309456-65309535 | Rare:20 | ||||
chr1:66533380-66533659 | Common:2; Rare:41 | ||||
chr1:66533846-66534196 | Common:2; Rare:85 | ||||
chr1:66924765-66925062 | Common:2; Rare:127 | ||||
chr1:66925160-66925518 | Common:2; Rare:114 | ||||
chr1:66930070-66930405 | Rare:106 | ||||
chr1:67053643-67054000 | Common:4; Rare:166; Clinvar (pathogenic):1 | ||||
chr1:67054134-67054169 | Rare:6 | ||||
chr1:67134936-67135071 | Common:1; Rare:34 | ||||
chr1:67429588-67429753 | Common:1; Rare:44 | ||||
chr1:67429991-67430072 | Rare:32 |