Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:40835181-40835418 | Common:2; Rare:95 | ||||
chr5:41925236-41925364 | Common:1; Rare:42 | ||||
chr5:43067422-43067561 | Rare:25 | ||||
chr5:43121406-43121648 | Common:1; Rare:93 | ||||
chr5:43313150-43313255 | Common:1; Rare:22 | ||||
chr5:43313393-43313670 | Common:3; Rare:74 | ||||
chr5:43483837-43483913 | Common:1; Rare:31 | ||||
chr5:43515133-43515356 | Common:3; Rare:74 | ||||
chr5:43603102-43603266 | Rare:39 | ||||
chr5:44808730-44808965 | Common:2; Rare:77 | ||||
chr5:51383258-51383448 | Common:2; Rare:69 | ||||
chr5:52989141-52989365 | Common:5; Rare:65; Clinvar (benign):1 | ||||
chr5:53109725-53109885 | Common:1; Rare:79; Clinvar:2 | ||||
chr5:54310507-54310711 | Rare:65 | ||||
chr5:55307620-55308025 | Common:4; Rare:139 |