Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228139837-228140083 | Common:1; Rare:59 | ||||
chr1:228457821-228458114 | Common:2; Rare:117 | ||||
chr1:229271011-229271331 | Rare:105 | ||||
chr1:229508272-229508445 | Common:1; Rare:69 | ||||
chr1:229625964-229626219 | Rare:72 | ||||
chr1:230978751-230979077 | Common:2; Rare:122 | ||||
chr1:231241110-231241362 | Common:2; Rare:123; Clinvar:4; Clinvar (benign):2 | ||||
chr1:231337831-231338056 | Common:2; Rare:81 | ||||
chr1:231528517-231528733 | Common:2; Rare:78 | ||||
chr1:234373419-234373582 | Common:1; Rare:85; Clinvar (benign):4 | ||||
chr1:234373618-234373780 | Rare:64; Clinvar (benign):3 | ||||
chr1:235128774-235129023 | Rare:99 | ||||
chr1:235866876-235867177 | Common:3; Rare:96 | ||||
chr1:236065037-236065353 | Common:3; Rare:119; Clinvar (pathogenic):1 | ||||
chr1:236523854-236524034 | Common:2; Rare:48 |