Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:225825184-225825544 | Common:1; Rare:81 | ||||
chr1:225882320-225882464 | Rare:44 | ||||
chr1:225924064-225924430 | Common:8; Rare:122 | ||||
chr1:225999313-225999618 | Common:2; Rare:103 | ||||
chr1:226062044-226062094 | Common:1; Rare:16 | ||||
chr1:226062539-226062835 | Rare:97 | ||||
chr1:226186391-226186779 | Common:1; Rare:109 | ||||
chr1:226309128-226309449 | Common:1; Rare:140 | ||||
chr1:226309761-226309849 | Common:1; Rare:25 | ||||
chr1:226870439-226870637 | Common:1; Rare:56; Clinvar (benign):1 | ||||
chr1:226939985-226940435 | Common:1; Rare:149; Clinvar:3; Clinvar (benign):1 | ||||
chr1:226982661-226983051 | Common:3; Rare:148; Clinvar:7; Clinvar (benign):8; Clinvar (pathogenic):6 | ||||
chr1:227728364-227728713 | Common:4; Rare:55 | ||||
chr1:227735198-227735499 | Common:5; Rare:172 | ||||
chr1:228082500-228082768 | Common:3; Rare:110 |