Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156135896-156136434 | Common:4; Rare:175; Clinvar:39; Clinvar (benign):24; Clinvar (pathogenic):15 | ||||
chr1:156137462-156137743 | Common:1; Rare:60; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
chr1:156193828-156194138 | Common:3; Rare:79 | ||||
chr1:156282785-156282935 | Common:1; Rare:42 | ||||
chr1:156338153-156338570 | Common:2; Rare:152 | ||||
chr1:156500768-156501134 | Common:1; Rare:133 | ||||
chr1:156591678-156591855 | Common:4; Rare:93 | ||||
chr1:156601410-156601686 | Common:2; Rare:81 | ||||
chr1:156705575-156705677 | Rare:24 | ||||
chr1:156728388-156728510 | Common:1; Rare:25 | ||||
chr1:156728533-156728892 | Common:1; Rare:105 | ||||
chr1:156729099-156729102 | Rare:1 | ||||
chr1:156741051-156741417 | Common:1; Rare:98 | ||||
chr1:156747111-156747371 | Common:3; Rare:34 | ||||
chr1:156750200-156750413 | Rare:49 |