Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:152717829-152717972 | Rare:61 | ||||
chr2:152717995-152718113 | Rare:35 | ||||
chr2:152718481-152718637 | Rare:61 | ||||
chr2:159516535-159516665 | Common:1; Rare:15 | ||||
chr2:159615225-159615343 | Common:2; Rare:28 | ||||
chr2:159615427-159615692 | Common:2; Rare:85 | ||||
chr2:159616439-159616567 | Rare:22 | ||||
chr2:159712256-159712290 | Rare:16 | ||||
chr2:159712345-159712625 | Common:2; Rare:101 | ||||
chr2:160493432-160493595 | Common:1; Rare:56 | ||||
chr2:161308355-161308690 | Common:2; Rare:72 | ||||
chr2:169509658-169510604 | Common:2; Rare:254; Clinvar:4; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
chr2:169514566-169514959 | Common:1; Rare:90; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr2:169584701-169584816 | Rare:30 | ||||
chr2:169694380-169694598 | Common:5; Rare:65 |