Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:169705297-169705517 | Common:1; Rare:44 | ||||
chr6:169789976-169790072 | Rare:31 | ||||
chr7:193591-193755 | Rare:71 | ||||
chr7:856126-856369 | Common:1; Rare:53 | ||||
chr7:1532803-1533011 | Common:1; Rare:51 | ||||
chr7:4134829-4134954 | Common:2; Rare:38 | ||||
chr7:11194684-11194762 | Common:1; Rare:13 | ||||
chr7:26193252-26193672 | Rare:147; Clinvar (benign):1 | ||||
chr7:27617781-27617942 | Common:1; Rare:33 | ||||
chr7:27641732-27641818 | Rare:18 | ||||
chr7:32728038-32728134 | Common:1; Rare:38 | ||||
chr7:35648451-35648675 | Common:1; Rare:42 | ||||
chr7:41465565-41465877 | Common:2; Rare:53 | ||||
chr7:41709112-41709425 | Common:1; Rare:58 | ||||
chr7:42888671-42888993 | Common:2; Rare:72 |