Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:21509242-21509435 | Rare:49 | ||||
chr1:22052559-22052770 | Common:2; Rare:75 | ||||
chr1:23344219-23344555 | Common:2; Rare:114 | ||||
chr1:23368188-23368523 | Common:1; Rare:96 | ||||
chr1:23368854-23369057 | Common:1; Rare:59 | ||||
chr1:23559389-23559651 | Common:1; Rare:112 | ||||
chr1:23691664-23691897 | Common:5; Rare:86; Clinvar:2; Clinvar (benign):3 | ||||
chr1:23778281-23778659 | Common:10; Rare:141 | ||||
chr1:23791066-23791247 | Rare:55 | ||||
chr1:23793539-23793671 | Rare:34 | ||||
chr1:23800723-23800959 | Common:1; Rare:84 | ||||
chr1:23825400-23825528 | Common:2; Rare:42; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23959641-23959850 | Common:2; Rare:55 | ||||
chr1:23980189-23980525 | Rare:89 | ||||
chr1:24413672-24413868 | Common:1; Rare:47 |