Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:47150470-47150570 | Common:3; Rare:36 | ||||
chr18:49813672-49814105 | Common:2; Rare:154 | ||||
chr18:50878943-50879235 | Common:4; Rare:97 | ||||
chr18:51030077-51030235 | Rare:49 | ||||
chr18:54357921-54358016 | Common:5; Rare:31 | ||||
chr18:62186948-62187310 | Common:5; Rare:101 | ||||
chr18:63367187-63367325 | Rare:47 | ||||
chr18:68715033-68715227 | Common:1; Rare:87 | ||||
chr18:70205672-70205804 | Common:3; Rare:49; Clinvar (benign):2 | ||||
chr18:74597811-74597881 | Common:1; Rare:19 | ||||
chr18:79679743-79679867 | Common:2; Rare:32 | ||||
chr19:572328-572604 | Rare:139 | ||||
chr19:582551-582767 | Common:5; Rare:84 | ||||
chr19:633497-633759 | Common:8; Rare:123 | ||||
chr19:663140-663482 | Common:2; Rare:138 |