Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:179623609-179623951 | Common:4; Rare:127 | ||||
chr5:179698588-179699091 | Common:4; Rare:177 | ||||
chr5:179806900-179807063 | Common:3; Rare:56 | ||||
chr5:179820731-179821141 | Common:5; Rare:152; Clinvar:9; Clinvar (benign):4 | ||||
chr5:179858797-179858958 | Rare:91 | ||||
chr5:180802775-180802980 | Common:8; Rare:80 | ||||
chr5:180810108-180810283 | Common:5; Rare:53 | ||||
chr5:180815532-180815683 | Rare:36 | ||||
chr5:181040121-181040293 | Rare:34 | ||||
chr5:181223132-181223341 | Rare:76 | ||||
chr5:181223633-181223750 | Common:3; Rare:28 | ||||
chr5:181243680-181243772 | Rare:24 | ||||
chr5:181261081-181261286 | Rare:71 | ||||
chr6:292000-292326 | Common:1; Rare:53 | ||||
chr6:292434-292542 | Rare:34 |