Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:24642890-24643348 | Common:2; Rare:151 | ||||
chr1:25232442-25232667 | Rare:92 | ||||
chr1:25246993-25247132 | Rare:43 | ||||
chr1:25247314-25247638 | Common:2; Rare:126 | ||||
chr1:25337839-25337951 | Rare:12 | ||||
chr1:25338214-25338487 | Common:2; Rare:89 | ||||
chr1:25819898-25820023 | Common:2; Rare:38 | ||||
chr1:25906406-25906590 | Rare:71 | ||||
chr1:26279908-26280201 | Rare:160 | ||||
chr1:26432091-26432422 | Common:5; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472127-26472528 | Common:5; Rare:122 | ||||
chr1:26473036-26473293 | Common:1; Rare:136 | ||||
chr1:26695732-26696026 | Common:1; Rare:99 | ||||
chr1:26787877-26788214 | Common:3; Rare:94; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26890229-26890359 | Common:1; Rare:50 |