Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:77461978-77462035 | Common:1; Rare:14 | ||||
chr6:77462741-77462789 | Rare:12 | ||||
chr6:77464279-77464512 | Common:1; Rare:69 | ||||
chr6:85678704-85678929 | Rare:80 | ||||
chr6:135358158-135358409 | Common:2; Rare:58; Clinvar (benign):1 | ||||
chr6:136793049-136793210 | Common:1; Rare:46 | ||||
chr6:157221363-157221471 | Common:2; Rare:35 | ||||
chr6:169162945-169163270 | Common:3; Rare:69 | ||||
chr7:5397224-5397321 | Rare:29 | ||||
chr7:16644739-16644922 | Rare:55 | ||||
chr7:27192198-27192230 | Rare:9 | ||||
chr7:32942496-32942648 | Common:1; Rare:41 | ||||
chr7:44019117-44019389 | Common:2; Rare:97 | ||||
chr7:44986592-44986766 | Common:2; Rare:87 | ||||
chr7:45768893-45769141 | Common:3; Rare:71 |