Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154975759-154975939 | Common:1; Rare:34 | ||||
chr1:154983121-154983402 | Common:2; Rare:55; Clinvar (benign):1 | ||||
chr1:155002110-155002354 | Common:1; Rare:69 | ||||
chr1:155050964-155051395 | Common:2; Rare:130 | ||||
chr1:155059950-155060343 | Common:2; Rare:111 | ||||
chr1:155063945-155064133 | Common:1; Rare:55 | ||||
chr1:155078703-155079011 | Common:2; Rare:91 | ||||
chr1:155127737-155127962 | Common:1; Rare:53 | ||||
chr1:155135716-155135914 | Common:3; Rare:83 | ||||
chr1:155138020-155138217 | Rare:57 | ||||
chr1:155192892-155193051 | Rare:40 | ||||
chr1:155209121-155209257 | Rare:61 | ||||
chr1:155236383-155236631 | Common:1; Rare:76; Clinvar (pathogenic):3 | ||||
chr1:155255427-155255587 | Common:1; Rare:32 | ||||
chr1:155262201-155262695 | Common:2; Rare:155 |