Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:106284978-106285225 | Common:2; Rare:87 | ||||
chr7:107563894-107563986 | Common:1; Rare:55; Clinvar (benign):1 | ||||
chr7:107744053-107744159 | Rare:36 | ||||
chr7:108569634-108569931 | Common:1; Rare:91 | ||||
chr7:116499435-116499790 | Common:3; Rare:118 | ||||
chr7:116524489-116524800 | Rare:72 | ||||
chr7:134646582-134646856 | Common:6; Rare:77 | ||||
chr7:141738043-141738455 | Common:4; Rare:130 | ||||
chr7:155644362-155644697 | Common:2; Rare:110 | ||||
chr8:232229-232448 | Common:2; Rare:92 | ||||
chr8:6406564-6406651 | Common:2; Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
chr8:10839866-10839982 | Rare:37 | ||||
chr8:17246826-17246982 | Common:1; Rare:63 | ||||
chr8:23457625-23457771 | Common:2; Rare:57 | ||||
chr8:26382937-26383119 | Common:1; Rare:86 |