Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:21887212-21887694 | Common:3; Rare:184; Clinvar:14; Clinvar (benign):3 | ||||
chr1:21889280-21889747 | Common:1; Rare:87 | ||||
chr1:21897543-21897609 | Rare:9 | ||||
chr1:21898884-21899087 | Rare:40 | ||||
chr1:21900269-21900580 | Common:2; Rare:42 | ||||
chr1:21906288-21906508 | Rare:45 | ||||
chr1:21910152-21910240 | Rare:20 | ||||
chr1:21916748-21916998 | Common:1; Rare:41 | ||||
chr1:21917098-21917103 | Rare:1 | ||||
chr1:21919451-21919616 | Rare:23 | ||||
chr1:21929580-21929618 | Rare:9 | ||||
chr1:21929630-21929835 | Common:2; Rare:51 | ||||
chr1:21929983-21930270 | Common:1; Rare:43 | ||||
chr1:21933253-21933552 | Common:2; Rare:66 | ||||
chr1:21933759-21934163 | Common:2; Rare:79 |