Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11274096-11274224 | Rare:25 | ||||
chr1:11478634-11478939 | Common:2; Rare:78 | ||||
chr1:11479067-11479209 | Common:4; Rare:55 | ||||
chr1:11653382-11653485 | Rare:14 | ||||
chr1:11654332-11654561 | Rare:58 | ||||
chr1:11654651-11655074 | Common:5; Rare:103 | ||||
chr1:11664247-11664427 | Rare:42 | ||||
chr1:11664703-11664771 | Rare:10 | ||||
chr1:11681078-11681211 | Rare:41 | ||||
chr1:11735949-11736202 | Common:3; Rare:76 | ||||
chr1:11736426-11736649 | Common:1; Rare:54 | ||||
chr1:11762047-11762085 | Rare:14 | ||||
chr1:11787595-11787736 | Common:3; Rare:34; Clinvar:2; Clinvar (benign):2 | ||||
chr1:11804874-11804979 | Rare:21 | ||||
chr1:11805447-11805626 | Common:2; Rare:34 |