Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:227728361-227728647 | Common:4; Rare:48 | ||||
chr1:227735237-227735493 | Common:3; Rare:150 | ||||
chr1:228103289-228103502 | Common:1; Rare:72 | ||||
chr1:228109239-228109502 | Rare:88 | ||||
chr1:228139928-228140375 | Common:3; Rare:144 | ||||
chr1:228166022-228166130 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr1:228457866-228458116 | Common:1; Rare:82 | ||||
chr1:229271024-229271166 | Rare:53 | ||||
chr1:229508308-229508449 | Common:1; Rare:52 | ||||
chr1:229626088-229626251 | Rare:55 | ||||
chr1:230978830-230979094 | Common:1; Rare:91 | ||||
chr1:231241087-231241277 | Rare:103; Clinvar:3 | ||||
chr1:231337809-231338051 | Common:2; Rare:89 | ||||
chr1:231528616-231528735 | Common:1; Rare:50 | ||||
chr1:233295716-233295799 | Common:1; Rare:24 |