Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:34976846-34977061 | Common:2; Rare:44 | ||||
chr18:35041238-35041440 | Common:1; Rare:70 | ||||
chr18:35240917-35241074 | Common:2; Rare:55 | ||||
chr18:35290193-35290384 | Common:2; Rare:68 | ||||
chr18:36129246-36129466 | Common:4; Rare:68 | ||||
chr18:36129868-36129928 | Rare:25 | ||||
chr18:36828748-36829138 | Common:3; Rare:144 | ||||
chr18:46072242-46072380 | Common:1; Rare:31 | ||||
chr18:46098235-46098550 | Common:11; Rare:90; Clinvar (benign):6 | ||||
chr18:46104135-46104408 | Common:4; Rare:80; Clinvar (benign):1 | ||||
chr18:46173924-46174081 | Common:1; Rare:43 | ||||
chr18:47150452-47150570 | Common:3; Rare:43 | ||||
chr18:49561879-49562093 | Rare:55 | ||||
chr18:49813835-49814199 | Common:1; Rare:153 | ||||
chr18:50878921-50879166 | Common:4; Rare:85 |