Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:29809968-29810206 | Common:6; Rare:142 | ||||
chr16:29845858-29846283 | Common:2; Rare:124 | ||||
chr16:30444498-30444599 | Rare:19 | ||||
chr16:30634282-30634559 | Common:1; Rare:71 | ||||
chr16:30756651-30756955 | Rare:121; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr16:30771913-30772189 | Common:1; Rare:78 | ||||
chr16:30875325-30875501 | Rare:59 | ||||
chr16:30918982-30919119 | Rare:30 | ||||
chr16:31037903-31037931 | Rare:8 | ||||
chr16:31189112-31189318 | Rare:38; Clinvar (pathogenic):1 | ||||
chr16:46803742-46803775 | Rare:5 | ||||
chr16:46963710-46963975 | Common:2; Rare:56 | ||||
chr16:47272441-47272493 | Rare:12 | ||||
chr16:48339521-48339673 | Rare:29 | ||||
chr16:48386276-48386461 | Rare:36 |