Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:13129752-13130018 | Rare:62 | ||||
chr8:13130888-13131061 | Common:3; Rare:42 | ||||
chr8:13366719-13366986 | Common:3; Rare:74 | ||||
chr8:13471770-13471893 | Rare:34 | ||||
chr8:17494183-17494365 | Rare:43 | ||||
chr8:18010987-18011288 | Common:3; Rare:77 | ||||
chr8:18057597-18057912 | Common:7; Rare:75; Clinvar (benign):1 | ||||
chr8:18083178-18083328 | Rare:47 | ||||
chr8:19235612-19235812 | Common:2; Rare:47 | ||||
chr8:19941461-19941797 | Common:1; Rare:58 | ||||
chr8:22392292-22392308 | Rare:1 | ||||
chr8:22525576-22525906 | Common:6; Rare:59 | ||||
chr8:22666876-22667171 | Rare:61 | ||||
chr8:23761522-23761802 | Common:1; Rare:67 | ||||
chr8:26407999-26408375 | Rare:97 |