Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10475360-10475436 | Common:1; Rare:18 | ||||
chr1:10693733-10693872 | Rare:41 | ||||
chr1:11011871-11011945 | Rare:18 | ||||
chr1:11012173-11012417 | Common:1; Rare:58 | ||||
chr1:11012595-11012756 | Common:1; Rare:48; Clinvar:4; Clinvar (benign):1 | ||||
chr1:11013002-11013136 | Rare:47 | ||||
chr1:11059905-11060470 | Common:4; Rare:178 | ||||
chr1:11099319-11099493 | Rare:44 | ||||
chr1:11099568-11099607 | Rare:10 | ||||
chr1:11099769-11100049 | Common:2; Rare:109 | ||||
chr1:11262457-11262914 | Common:3; Rare:134 | ||||
chr1:11272916-11273338 | Common:2; Rare:116; Clinvar:1; Clinvar (benign):2 | ||||
chr1:11273390-11273727 | Common:1; Rare:105; Clinvar:3; Clinvar (benign):1 | ||||
chr1:11479105-11479185 | Common:3; Rare:36 | ||||
chr1:11654739-11655058 | Common:4; Rare:78 |