Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:44531605-44531774 | Rare:40 | ||||
chr18:44579942-44580034 | Rare:16 | ||||
chr18:45507029-45507206 | Common:1; Rare:39 | ||||
chr18:46028150-46028344 | Rare:61 | ||||
chr18:46087208-46087441 | Rare:53; Clinvar (pathogenic):1 | ||||
chr18:46389508-46389631 | Rare:31 | ||||
chr18:46560501-46560682 | Rare:61; Clinvar (benign):1 | ||||
chr18:47501077-47501194 | Rare:23 | ||||
chr18:47668064-47668217 | Rare:24 | ||||
chr18:47754421-47754444 | Rare:5 | ||||
chr18:47992036-47992231 | Common:1; Rare:33 | ||||
chr18:48252604-48252798 | Common:3; Rare:34 | ||||
chr18:48362308-48362460 | Common:2; Rare:31 | ||||
chr18:48662657-48662967 | Common:1; Rare:71 | ||||
chr18:49016574-49016698 | Rare:21 |