Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25859370-25859580 | Common:2; Rare:85 | ||||
chr1:25906392-25906591 | Rare:77 | ||||
chr1:26279934-26280156 | Rare:125 | ||||
chr1:26432100-26432414 | Common:5; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472272-26472532 | Common:4; Rare:84 | ||||
chr1:26787870-26788214 | Common:3; Rare:98; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26900428-26900524 | Rare:38 | ||||
chr1:26921556-26921825 | Common:3; Rare:85 | ||||
chr1:26960377-26960533 | Common:1; Rare:31 | ||||
chr1:27322073-27322330 | Common:1; Rare:98 | ||||
chr1:27725762-27725998 | Common:2; Rare:63 | ||||
chr1:27772993-27773315 | Common:1; Rare:112 | ||||
chr1:28088541-28088818 | Common:3; Rare:97 | ||||
chr1:28236058-28236201 | Common:1; Rare:55 | ||||
chr1:28328902-28329079 | Common:1; Rare:53 |