Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:22451602-22451868 | Common:1; Rare:76 | ||||
chr1:23424630-23424879 | Common:1; Rare:76 | ||||
chr1:23559440-23559643 | Common:1; Rare:90 | ||||
chr1:23691571-23691826 | Common:3; Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
chr1:23778288-23778525 | Common:9; Rare:120 | ||||
chr1:23800745-23800929 | Common:1; Rare:58 | ||||
chr1:23825403-23825545 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23980251-23980495 | Rare:76 | ||||
chr1:24112105-24112312 | Rare:58 | ||||
chr1:24415538-24415827 | Common:2; Rare:76 | ||||
chr1:25232444-25232596 | Rare:62 | ||||
chr1:25247445-25247638 | Common:2; Rare:69 | ||||
chr1:25338232-25338487 | Common:2; Rare:83 | ||||
chr1:25819875-25820209 | Common:4; Rare:100 | ||||
chr1:26067506-26067829 | Common:2; Rare:57 |