Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:230868830-230869044 | Rare:33 | ||||
chr1:230978748-230979138 | Common:2; Rare:153 | ||||
chr1:231241104-231241367 | Common:2; Rare:130; Clinvar:4; Clinvar (benign):2 | ||||
chr1:231337819-231338056 | Common:2; Rare:86 | ||||
chr1:231528521-231528738 | Common:2; Rare:77 | ||||
chr1:234373377-234373554 | Common:1; Rare:94; Clinvar (benign):3 | ||||
chr1:234373625-234373780 | Rare:60; Clinvar (benign):3 | ||||
chr1:235328116-235328408 | Common:2; Rare:85 | ||||
chr1:236064931-236065360 | Common:4; Rare:151; Clinvar (pathogenic):1 | ||||
chr1:236281936-236282258 | Common:6; Rare:95 | ||||
chr1:236523616-236524036 | Common:5; Rare:101 | ||||
chr1:236604466-236604645 | Common:4; Rare:52 | ||||
chr1:239386492-239386697 | Rare:31 | ||||
chr1:243255040-243255355 | Common:1; Rare:72 | ||||
chr1:243255430-243255548 | Rare:20 |