Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154974314-154974742 | Rare:113 | ||||
chr1:154983102-154983400 | Common:2; Rare:59; Clinvar (benign):1 | ||||
chr1:155002103-155002354 | Common:1; Rare:73 | ||||
chr1:155002397-155002926 | Common:3; Rare:80 | ||||
chr1:155051150-155051401 | Common:2; Rare:82 | ||||
chr1:155063966-155064130 | Common:1; Rare:42 | ||||
chr1:155127548-155127962 | Common:1; Rare:84 | ||||
chr1:155129195-155129271 | Rare:13 | ||||
chr1:155135231-155135424 | Rare:44 | ||||
chr1:155135703-155135948 | Common:3; Rare:101 | ||||
chr1:155138034-155138245 | Rare:56 | ||||
chr1:155187427-155187896 | Common:3; Rare:137 | ||||
chr1:155192708-155193051 | Rare:94 | ||||
chr1:155193342-155193527 | Rare:33 | ||||
chr1:155207852-155208042 | Rare:52 |