Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:20661348-20661752 | Common:3; Rare:147; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20732040-20732430 | Common:1; Rare:89 | ||||
chr1:20732990-20733450 | Common:6; Rare:92 | ||||
chr1:20786579-20786922 | Rare:130 | ||||
chr1:20787257-20787460 | Rare:97 | ||||
chr1:21176815-21177081 | Rare:74 | ||||
chr1:21289830-21290170 | Common:2; Rare:100 | ||||
chr1:21290370-21290920 | Common:5; Rare:120 | ||||
chr1:21345452-21345755 | Common:3; Rare:99 | ||||
chr1:21439985-21440242 | Common:2; Rare:56 | ||||
chr1:21509218-21509483 | Rare:72 | ||||
chr1:21622509-21622715 | Common:4; Rare:69 | ||||
chr1:21651590-21651990 | Common:1; Rare:165 | ||||
chr1:21782164-21782564 | Common:2; Rare:90 | ||||
chr1:21782834-21783335 | Common:4; Rare:165 |