Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:46048398-46048628 | Common:3; Rare:48 | ||||
chr22:46069860-46070098 | Rare:54 | ||||
chr22:46085841-46086036 | Common:2; Rare:45 | ||||
chr22:47487056-47487186 | Rare:38 | ||||
chr3:4751616-4751776 | Common:2; Rare:31 | ||||
chr3:4868556-4868663 | Rare:43 | ||||
chr3:4978344-4978569 | Common:1; Rare:67 | ||||
chr3:9396237-9396322 | Rare:39 | ||||
chr3:9396638-9396705 | Rare:29 | ||||
chr3:15259770-15260067 | Common:2; Rare:86 | ||||
chr3:30688109-30688471 | Common:2; Rare:80; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr3:40453171-40453421 | Common:5; Rare:53 | ||||
chr3:41225600-41225727 | Rare:23 | ||||
chr3:41237751-41238072 | Common:1; Rare:82; Clinvar (pathogenic):1 | ||||
chr3:42632242-42632693 | Common:2; Rare:93 |