Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25247441-25247621 | Common:2; Rare:59 | ||||
chr1:25819879-25820237 | Common:5; Rare:106 | ||||
chr1:25859351-25859580 | Common:3; Rare:97 | ||||
chr1:25892564-25892693 | Common:3; Rare:25 | ||||
chr1:26110964-26111147 | Common:2; Rare:62 | ||||
chr1:26187202-26187391 | Rare:46 | ||||
chr1:26278769-26279090 | Common:4; Rare:69 | ||||
chr1:26279934-26280204 | Rare:144 | ||||
chr1:26432073-26432413 | Common:5; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26529569-26529809 | Common:3; Rare:82 | ||||
chr1:26695941-26696063 | Rare:41 | ||||
chr1:26766140-26766262 | Common:1; Rare:34; Clinvar (pathogenic):1 | ||||
chr1:26787829-26788006 | Common:3; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26890229-26890523 | Common:1; Rare:116 | ||||
chr1:26899998-26900220 | Rare:87 |