Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:66925192-66925518 | Common:2; Rare:101 | ||||
chr1:66930192-66930405 | Rare:70 | ||||
chr1:66958782-66958902 | Common:1; Rare:33 | ||||
chr1:67053603-67053782 | Common:4; Rare:72 | ||||
chr1:67053919-67054175 | Common:1; Rare:96 | ||||
chr1:67429989-67430551 | Rare:204 | ||||
chr1:67833335-67833504 | Common:2; Rare:68 | ||||
chr1:68232400-68232621 | Common:1; Rare:47 | ||||
chr1:70205496-70205796 | Rare:105 | ||||
chr1:70221316-70221614 | Rare:117 | ||||
chr1:70249854-70250685 | Common:1; Rare:211 | ||||
chr1:70354573-70354863 | Common:1; Rare:85 | ||||
chr1:70411089-70411285 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71047123-71047256 | Rare:39 | ||||
chr1:71080945-71081387 | Rare:120 |