Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153775025-153775412 | Common:1; Rare:168 | ||||
chr1:153933312-153933379 | Rare:13 | ||||
chr1:153963460-153963745 | Common:2; Rare:80 | ||||
chr1:153967301-153967564 | Common:1; Rare:56 | ||||
chr1:153967710-153967937 | Rare:45 | ||||
chr1:153968149-153968289 | Common:1; Rare:22 | ||||
chr1:153977981-153978253 | Rare:51 | ||||
chr1:153985388-153985531 | Rare:22 | ||||
chr1:153986114-153986449 | Rare:87 | ||||
chr1:153990663-153990826 | Common:2; Rare:80 | ||||
chr1:154172906-154173217 | Common:1; Rare:57; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:154182616-154182881 | Common:1; Rare:55 | ||||
chr1:154182986-154183231 | Rare:82 | ||||
chr1:154183234-154183266 | Rare:6 | ||||
chr1:154219841-154220251 | Common:5; Rare:114 |