Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:44678356-44678706 | Common:1; Rare:128 | ||||
chr4:44726547-44726659 | Rare:48 | ||||
chr4:47463623-47463779 | Common:1; Rare:57 | ||||
chr4:47485191-47485353 | Common:1; Rare:59 | ||||
chr4:47914520-47914865 | Common:1; Rare:107 | ||||
chr4:48341284-48341478 | Rare:83 | ||||
chr4:52038240-52038346 | Rare:45; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr4:52659209-52659439 | Common:1; Rare:78 | ||||
chr4:55346188-55346332 | Common:3; Rare:48; Clinvar:3; Clinvar (benign):2 | ||||
chr4:55546816-55547011 | Common:2; Rare:68 | ||||
chr4:56387423-56387516 | Rare:32 | ||||
chr4:56435551-56436307 | Common:4; Rare:249 | ||||
chr4:56467555-56467654 | Rare:38 | ||||
chr4:56977581-56977785 | Common:1; Rare:75 | ||||
chr4:67545455-67545746 | Common:2; Rare:75 |