Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:225428016-225428329 | Common:3; Rare:99; Clinvar:2; Clinvar (benign):2 | ||||
chr1:225777741-225777887 | Common:3; Rare:39 | ||||
chr1:225809953-225810129 | Common:4; Rare:36 | ||||
chr1:225999316-225999618 | Common:2; Rare:101 | ||||
chr1:226870554-226870637 | Common:1; Rare:29; Clinvar (benign):1 | ||||
chr1:226939985-226940360 | Rare:131; Clinvar:3 | ||||
chr1:227735231-227735471 | Common:3; Rare:138 | ||||
chr1:228103317-228103442 | Common:1; Rare:42 | ||||
chr1:228139841-228140083 | Common:1; Rare:58 | ||||
chr1:228457857-228458113 | Common:1; Rare:83 | ||||
chr1:229271020-229271301 | Rare:94 | ||||
chr1:229433976-229434480 | Common:6; Rare:121; Clinvar (benign):2 | ||||
chr1:229508275-229508440 | Common:1; Rare:68 | ||||
chr1:231241112-231241238 | Rare:65; Clinvar:2 | ||||
chr1:231337819-231338056 | Common:2; Rare:86 |