Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:224434795-224434892 | Rare:27 | ||||
chr1:225404418-225404659 | Rare:73; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr1:225427957-225428302 | Common:3; Rare:120; Clinvar:5; Clinvar (benign):3 | ||||
chr1:225999305-225999622 | Common:2; Rare:108 | ||||
chr1:226062493-226062814 | Rare:112 | ||||
chr1:226063669-226063924 | Common:1; Rare:72 | ||||
chr1:226186405-226186813 | Common:1; Rare:116 | ||||
chr1:226939984-226940343 | Rare:122; Clinvar:3 | ||||
chr1:227735253-227735491 | Common:2; Rare:139 | ||||
chr1:228103322-228103497 | Common:1; Rare:56 | ||||
chr1:228109205-228109502 | Rare:93 | ||||
chr1:228165416-228165590 | Rare:58 | ||||
chr1:228166026-228166345 | Common:1; Rare:129; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
chr1:228457863-228458144 | Common:1; Rare:106 | ||||
chr1:229271014-229271351 | Rare:107 |