Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23868259-23868445 | Common:5; Rare:61; Clinvar:1; Clinvar (benign):4 | ||||
chr1:23959608-23959892 | Common:2; Rare:78 | ||||
chr1:23980251-23980525 | Rare:86 | ||||
chr1:24112099-24112334 | Rare:65 | ||||
chr1:25232448-25232596 | Rare:59 | ||||
chr1:25247434-25247638 | Common:2; Rare:74 | ||||
chr1:25338214-25338494 | Common:2; Rare:91 | ||||
chr1:25819895-25820253 | Common:5; Rare:105 | ||||
chr1:26257319-26257537 | Common:4; Rare:36 | ||||
chr1:26279934-26280201 | Rare:144 | ||||
chr1:26432119-26432422 | Common:4; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26787877-26788214 | Common:3; Rare:94; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26890211-26890347 | Common:1; Rare:50 | ||||
chr1:26900441-26900524 | Rare:32 | ||||
chr1:26921554-26921926 | Common:3; Rare:115 |