Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:46797098-46797362 | Common:3; Rare:87 | ||||
chr13:48001253-48001410 | Common:1; Rare:72; Clinvar:3; Clinvar (benign):3 | ||||
chr13:48037423-48037789 | Common:2; Rare:141 | ||||
chr13:48037920-48038090 | Common:5; Rare:56 | ||||
chr13:48095034-48095228 | Common:2; Rare:95 | ||||
chr13:48233060-48233182 | Common:1; Rare:32 | ||||
chr13:48233252-48233475 | Common:2; Rare:71 | ||||
chr13:48303665-48304017 | Common:1; Rare:120; Clinvar:12; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr13:48533046-48533129 | Common:1; Rare:27 | ||||
chr13:48653532-48653852 | Rare:56 | ||||
chr13:48975800-48975960 | Rare:59 | ||||
chr13:48976154-48976246 | Rare:26 | ||||
chr13:48976540-48976849 | Common:1; Rare:88 | ||||
chr13:49110216-49110397 | Common:2; Rare:56 | ||||
chr13:49247782-49247976 | Rare:53 |