Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43979880-43980006 | Common:2; Rare:31 | ||||
chr1:44213326-44213498 | Common:1; Rare:35 | ||||
chr1:44674425-44674733 | Common:3; Rare:76 | ||||
chr1:44775462-44775607 | Rare:55 | ||||
chr1:44775843-44776138 | Common:2; Rare:107 | ||||
chr1:45339957-45340041 | Rare:29 | ||||
chr1:45340111-45340182 | Rare:26 | ||||
chr1:45500046-45500335 | Common:1; Rare:68; Clinvar:4; Clinvar (pathogenic):2 | ||||
chr1:45521859-45522074 | Common:1; Rare:85 | ||||
chr1:45550719-45551110 | Common:3; Rare:96 | ||||
chr1:45583940-45584114 | Rare:68 | ||||
chr1:45687059-45687353 | Common:1; Rare:77 | ||||
chr1:45688091-45688243 | Common:1; Rare:48 | ||||
chr1:45750618-45750821 | Rare:77 | ||||
chr1:46198389-46198506 | Common:1; Rare:46; Clinvar:1 |