Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:45967261-45967508 | Rare:92 | ||||
chr18:46098218-46098548 | Common:11; Rare:99; Clinvar (benign):6 | ||||
chr18:46104135-46104420 | Common:4; Rare:85; Clinvar (benign):1 | ||||
chr18:47150435-47150570 | Common:3; Rare:51 | ||||
chr18:47930781-47931018 | Rare:77 | ||||
chr18:48137048-48137202 | Rare:31 | ||||
chr18:49487143-49487328 | Common:3; Rare:74 | ||||
chr18:49813826-49814303 | Common:2; Rare:194 | ||||
chr18:49849804-49849988 | Rare:45 | ||||
chr18:50281426-50281840 | Common:3; Rare:129 | ||||
chr18:50879011-50879235 | Common:4; Rare:75 | ||||
chr18:51030063-51030222 | Rare:51 | ||||
chr18:54269467-54269622 | Common:2; Rare:79 | ||||
chr18:54357873-54357955 | Common:3; Rare:22 | ||||
chr18:54828326-54828530 | Rare:50 |