Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42587058-42587113 | Rare:6 | ||||
chr17:42608858-42609125 | Common:1; Rare:73 | ||||
chr17:42609142-42609182 | Rare:17 | ||||
chr17:42609271-42609843 | Common:9; Rare:221; Clinvar (benign):2 | ||||
chr17:42659143-42659490 | Rare:104 | ||||
chr17:42676889-42677506 | Common:1; Rare:141 | ||||
chr17:42681747-42681962 | Rare:52 | ||||
chr17:42682368-42682768 | Common:3; Rare:78 | ||||
chr17:42683608-42683844 | Common:2; Rare:44 | ||||
chr17:42744383-42744557 | Common:1; Rare:40 | ||||
chr17:42744634-42744817 | Rare:38 | ||||
chr17:42744955-42745209 | Common:3; Rare:98 | ||||
chr17:42773309-42773586 | Rare:79 | ||||
chr17:42798610-42798740 | Rare:54 | ||||
chr17:42824163-42824481 | Common:2; Rare:88 |