Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:46098218-46098550 | Common:11; Rare:99; Clinvar (benign):6 | ||||
chr18:46104136-46104399 | Common:3; Rare:75; Clinvar (benign):1 | ||||
chr18:47150452-47150546 | Common:2; Rare:34 | ||||
chr18:48539002-48539192 | Common:1; Rare:45 | ||||
chr18:49487212-49487328 | Common:1; Rare:43 | ||||
chr18:49490452-49490915 | Common:1; Rare:114 | ||||
chr18:49813826-49814180 | Common:1; Rare:144 | ||||
chr18:50281426-50281847 | Common:3; Rare:132 | ||||
chr18:55321703-55321921 | Rare:48 | ||||
chr18:55401748-55402018 | Rare:47 | ||||
chr18:55588095-55588337 | Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
chr18:55589713-55590011 | Common:2; Rare:99 | ||||
chr18:56651133-56651379 | Common:3; Rare:62 | ||||
chr18:57621724-57621948 | Common:2; Rare:81 | ||||
chr18:62186945-62187297 | Common:5; Rare:97 |