Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11274051-11274184 | Rare:34; Clinvar (pathogenic):2 | ||||
chr1:11654327-11654464 | Rare:37 | ||||
chr1:11654694-11655060 | Common:5; Rare:87 | ||||
chr1:11664126-11664380 | Rare:67 | ||||
chr1:11680696-11680748 | Rare:19 | ||||
chr1:11681061-11681343 | Common:2; Rare:101 | ||||
chr1:11681459-11681547 | Common:1; Rare:13 | ||||
chr1:11735953-11736230 | Common:3; Rare:81 | ||||
chr1:11736427-11736678 | Common:1; Rare:59 | ||||
chr1:11803119-11803225 | Common:1; Rare:33; Clinvar (pathogenic):1 | ||||
chr1:11803502-11803798 | Common:1; Rare:62 | ||||
chr1:11804861-11805042 | Common:1; Rare:30 | ||||
chr1:11805431-11805787 | Common:5; Rare:79 | ||||
chr1:11805791-11806278 | Common:2; Rare:131; Clinvar:2 | ||||
chr1:11806347-11806508 | Common:2; Rare:36 |