Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:36155970-36156202 | Rare:100 | ||||
chr1:36385891-36386194 | Rare:85 | ||||
chr1:37474357-37474581 | Common:1; Rare:90 | ||||
chr1:37692193-37692570 | Common:4; Rare:89 | ||||
chr1:37807697-37807797 | Rare:37 | ||||
chr1:37808158-37808633 | Common:2; Rare:122 | ||||
chr1:37859590-37859747 | Common:2; Rare:53 | ||||
chr1:37989975-37990217 | Rare:78 | ||||
chr1:38012524-38012826 | Rare:91 | ||||
chr1:38873312-38873438 | Common:2; Rare:51 | ||||
chr1:39883450-39883593 | Common:1; Rare:59; Clinvar (pathogenic):1 | ||||
chr1:39955004-39955147 | Common:1; Rare:32 | ||||
chr1:40040302-40040810 | Common:3; Rare:150 | ||||
chr1:40161254-40161405 | Rare:39 | ||||
chr1:40257915-40258373 | Common:4; Rare:132; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):2 |