Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:40688548-40688561 | Rare:2 | ||||
chr20:45424218-45424575 | Common:3; Rare:105; Clinvar (pathogenic):1 | ||||
chr20:45894650-45895032 | Common:3; Rare:136; Clinvar:3; Clinvar (benign):2 | ||||
chr20:45899460-45899713 | Rare:89 | ||||
chr20:45902265-45902603 | Common:1; Rare:120 | ||||
chr20:45904798-45905106 | Rare:101 | ||||
chr20:45946451-45946667 | Common:1; Rare:42 | ||||
chr20:47352496-47352565 | Rare:12 | ||||
chr20:47352571-47352664 | Rare:15 | ||||
chr20:47357783-47357908 | Rare:19 | ||||
chr20:48681288-48681582 | Rare:66 | ||||
chr20:49775349-49775603 | Common:2; Rare:43 | ||||
chr20:50166069-50166250 | Rare:46 | ||||
chr20:50172327-50172596 | Common:1; Rare:66 | ||||
chr20:50192207-50192437 | Common:2; Rare:56 |