Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23369806-23369963 | Rare:28 | ||||
chr1:23559011-23559154 | Common:2; Rare:65 | ||||
chr1:23559182-23559259 | Rare:29 | ||||
chr1:23559353-23559643 | Common:1; Rare:125 | ||||
chr1:23559840-23560097 | Common:1; Rare:78 | ||||
chr1:23691749-23691836 | Common:1; Rare:42; Clinvar:2; Clinvar (benign):1 | ||||
chr1:23778281-23778580 | Common:10; Rare:128 | ||||
chr1:23793554-23793639 | Rare:24 | ||||
chr1:23800753-23800929 | Common:1; Rare:56 | ||||
chr1:23959641-23959868 | Common:2; Rare:63 | ||||
chr1:23980190-23980486 | Rare:76 | ||||
chr1:24413697-24413903 | Common:1; Rare:49 | ||||
chr1:24415633-24415889 | Common:1; Rare:63 | ||||
chr1:24745281-24745556 | Common:2; Rare:96 | ||||
chr1:25232442-25232657 | Rare:87 |