Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:93078950-93079290 | Common:3; Rare:132 | ||||
chr1:93180110-93180186 | Rare:25 | ||||
chr1:93180199-93180754 | Common:2; Rare:220 | ||||
chr1:93345774-93345946 | Common:4; Rare:66 | ||||
chr1:93447996-93448252 | Common:2; Rare:84 | ||||
chr1:93879096-93879274 | Common:1; Rare:69 | ||||
chr1:94418226-94418470 | Common:2; Rare:85 | ||||
chr1:94541623-94542034 | Common:1; Rare:115 | ||||
chr1:94820126-94820440 | Common:4; Rare:78 | ||||
chr1:94926842-94927043 | Common:3; Rare:53 | ||||
chr1:94927048-94927450 | Common:1; Rare:133 | ||||
chr1:95072863-95073018 | Common:1; Rare:61; Clinvar (benign):1 | ||||
chr1:95233951-95234248 | Common:5; Rare:93 | ||||
chr1:97920991-97921156 | Rare:74; Clinvar:3 | ||||
chr1:99969916-99970074 | Rare:44 |