Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:38499082-38499114 | Rare:4 | ||||
chr3:39083018-39083245 | Common:2; Rare:37 | ||||
chr3:39144640-39144790 | Common:2; Rare:31 | ||||
chr3:39152695-39152790 | Rare:24 | ||||
chr3:39407506-39407643 | Rare:46 | ||||
chr3:40453149-40453484 | Common:7; Rare:76 | ||||
chr3:40461260-40461426 | Common:2; Rare:43 | ||||
chr3:41215965-41216031 | Rare:18 | ||||
chr3:41225154-41225567 | Rare:103; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr3:41683105-41683298 | Common:2; Rare:40 | ||||
chr3:42133584-42133592 | Rare:2 | ||||
chr3:42215126-42215395 | Rare:55 | ||||
chr3:42652750-42652945 | Rare:36 | ||||
chr3:42654386-42654656 | Rare:76 | ||||
chr3:43190722-43190968 | Common:2; Rare:50 |