Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26432073-26432422 | Common:5; Rare:89; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26473047-26473251 | Rare:104 | ||||
chr1:26787865-26788207 | Common:3; Rare:94; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26890234-26890377 | Common:1; Rare:61 | ||||
chr1:26900441-26900544 | Rare:34 | ||||
chr1:27725679-27726072 | Common:4; Rare:119 | ||||
chr1:28088565-28088818 | Common:3; Rare:89 | ||||
chr1:28232921-28233068 | Common:1; Rare:63 | ||||
chr1:28328894-28329073 | Common:1; Rare:57 | ||||
chr1:28505848-28506050 | Common:1; Rare:84 | ||||
chr1:28552882-28553127 | Common:2; Rare:95 | ||||
chr1:28643020-28643188 | Rare:65 | ||||
chr1:28736760-28737049 | Common:2; Rare:104 | ||||
chr1:28737660-28737750 | Rare:37 | ||||
chr1:29181754-29182145 | Common:3; Rare:155 |