Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11272922-11273223 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
chr1:11654396-11654493 | Rare:27 | ||||
chr1:11654705-11654909 | Common:4; Rare:57 | ||||
chr1:11805896-11806250 | Common:2; Rare:98; Clinvar:1 | ||||
chr1:11934576-11934743 | Common:2; Rare:57; Clinvar:5 | ||||
chr1:11979894-11980339 | Common:3; Rare:111; Clinvar:1; Clinvar (benign):1 | ||||
chr1:12618124-12618444 | Common:2; Rare:67 | ||||
chr1:13584136-13584298 | Common:2; Rare:56 | ||||
chr1:15526600-15526889 | Common:2; Rare:89 | ||||
chr1:15617188-15617443 | Common:2; Rare:72 | ||||
chr1:16133975-16134137 | Common:2; Rare:29 | ||||
chr1:16155856-16156177 | Rare:75; Clinvar:2 | ||||
chr1:17439707-17439873 | Rare:55 | ||||
chr1:18955770-18956026 | Rare:63 | ||||
chr1:19081447-19081748 | Common:3; Rare:102 |