Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:47592636-47592873 | Rare:52 | ||||
chr8:47736977-47737217 | Common:2; Rare:55 | ||||
chr8:47798304-47798525 | Common:3; Rare:42; Clinvar:1; Clinvar (benign):2 | ||||
chr8:47822330-47822471 | Rare:29 | ||||
chr8:47962839-47962984 | Rare:45; Clinvar:1 | ||||
chr8:49535792-49535961 | Rare:34 | ||||
chr8:52940818-52940867 | Common:1; Rare:23 | ||||
chr8:54049933-54050054 | Rare:23 | ||||
chr8:58145752-58145974 | Rare:41 | ||||
chr8:58982791-58982898 | Common:1; Rare:22 | ||||
chr8:60652256-60652480 | Common:4; Rare:79 | ||||
chr8:60921807-60921947 | Common:1; Rare:33 | ||||
chr8:61202560-61202855 | Common:2; Rare:60 | ||||
chr8:61639863-61639954 | Rare:24 | ||||
chr8:64114425-64114565 | Common:1; Rare:21 |