Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:236604453-236604616 | Common:4; Rare:53 | ||||
chr1:236795071-236795507 | Common:7; Rare:177; Clinvar:5; Clinvar (benign):1 | ||||
chr1:241848078-241848257 | Common:2; Rare:37 | ||||
chr1:243255045-243255365 | Common:1; Rare:73 | ||||
chr1:243255370-243255497 | Rare:30 | ||||
chr1:243255747-243256137 | Common:1; Rare:112; Clinvar:4; Clinvar (benign):1 | ||||
chr1:244451751-244452228 | Common:1; Rare:159 | ||||
chr1:244461300-244461342 | Common:1; Rare:12 | ||||
chr1:244835051-244835338 | Rare:106 | ||||
chr1:244835575-244835729 | Common:2; Rare:67; Clinvar (benign):4 | ||||
chr1:244856424-244856860 | Common:1; Rare:89; Clinvar (benign):2 | ||||
chr1:244863957-244864682 | Common:1; Rare:242; Clinvar:3; Clinvar (benign):6 | ||||
chr1:244970255-244970413 | Common:3; Rare:73 | ||||
chr1:246566160-246566606 | Common:3; Rare:150 | ||||
chr1:247078741-247078877 | Rare:42 |