Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:209616734-209616792 | Rare:8 | ||||
chr1:209617141-209617649 | Common:1; Rare:147; Clinvar:5; Clinvar (pathogenic):1 | ||||
chr1:209621752-209621927 | Rare:28 | ||||
chr1:209622088-209622290 | Common:1; Rare:31 | ||||
chr1:209624945-209625164 | Common:2; Rare:48 | ||||
chr1:209626383-209626400 | Rare:1 | ||||
chr1:209626493-209626586 | Common:2; Rare:15 | ||||
chr1:209626777-209627003 | Common:2; Rare:85; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:209629386-209629464 | Rare:14 | ||||
chr1:209632532-209633160 | Common:3; Rare:178; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
chr1:209633561-209633948 | Common:10; Rare:72 | ||||
chr1:209634216-209634891 | Common:5; Rare:168; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
chr1:209635077-209635371 | Common:1; Rare:56 | ||||
chr1:209636038-209636515 | Common:4; Rare:81 | ||||
chr1:209636524-209636920 | Common:2; Rare:79 |