Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11012232-11012366 | Rare:32 | ||||
chr1:11059994-11060294 | Common:3; Rare:89 | ||||
chr1:11099355-11099505 | Rare:36 | ||||
chr1:11099769-11100041 | Common:2; Rare:107 | ||||
chr1:11262528-11262959 | Common:2; Rare:118 | ||||
chr1:11272875-11273272 | Common:1; Rare:113; Clinvar:1; Clinvar (benign):1 | ||||
chr1:11654329-11654561 | Rare:58 | ||||
chr1:11654806-11654925 | Common:2; Rare:34 | ||||
chr1:11663870-11664320 | Common:2; Rare:113 | ||||
chr1:11664371-11665002 | Common:12; Rare:301 | ||||
chr1:11680830-11681470 | Common:6; Rare:184 | ||||
chr1:11681500-11681741 | Common:2; Rare:59 | ||||
chr1:11690590-11691260 | Common:5; Rare:132 | ||||
chr1:11736020-11736205 | Common:3; Rare:56 | ||||
chr1:11736489-11736603 | Rare:24 |