Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:50866348-50866587 | Common:3; Rare:73 | ||||
chr17:51120734-51120979 | Rare:99 | ||||
chr17:51166273-51166579 | Common:3; Rare:74 | ||||
chr17:51166681-51166955 | Rare:80 | ||||
chr17:51260362-51260611 | Common:3; Rare:119 | ||||
chr17:54968619-54968799 | Common:3; Rare:86 | ||||
chr17:56833896-56834191 | Common:2; Rare:100 | ||||
chr17:56913995-56914186 | Common:1; Rare:54 | ||||
chr17:57084959-57085339 | Common:1; Rare:126 | ||||
chr17:57850002-57850274 | Common:1; Rare:89 | ||||
chr17:57988154-57988519 | Common:5; Rare:108 | ||||
chr17:58692530-58692678 | Common:1; Rare:81; Clinvar:15; Clinvar (benign):20 | ||||
chr17:59106648-59106952 | Common:3; Rare:93; Clinvar:6; Clinvar (benign):4 | ||||
chr17:59155101-59155789 | Common:2; Rare:177 | ||||
chr17:59331491-59331778 | Common:2; Rare:94 |