Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:53873401-53873554 | Rare:36 | ||||
chr19:53876404-53876560 | Common:1; Rare:32 | ||||
chr19:53889580-53889900 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):11 | ||||
chr19:53979370-53979595 | Rare:35 | ||||
chr19:53980242-53980456 | Common:4; Rare:58 | ||||
chr19:53980733-53981135 | Common:3; Rare:83 | ||||
chr19:53981315-53981497 | Rare:40 | ||||
chr19:53991379-53991658 | Common:6; Rare:59 | ||||
chr19:54096645-54096833 | Common:5; Rare:33 | ||||
chr19:55006049-55006254 | Common:3; Rare:91 | ||||
chr19:55189470-55189602 | Common:3; Rare:40 | ||||
chr19:55369771-55369800 | Common:1; Rare:6 | ||||
chr19:55383648-55383965 | Common:1; Rare:74 | ||||
chr19:55547302-55547471 | Common:2; Rare:30 | ||||
chr19:55580137-55580284 | Common:2; Rare:25 |