Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:157138363-157138655 | Common:3; Rare:91 | ||||
chr1:158999700-159000033 | Common:2; Rare:72 | ||||
chr1:159924561-159924734 | Rare:41 | ||||
chr1:160343181-160343415 | Rare:96 | ||||
chr1:161045888-161046042 | Common:1; Rare:39 | ||||
chr1:161118008-161118136 | Rare:61 | ||||
chr1:161132592-161132627 | Common:1; Rare:10 | ||||
chr1:161199053-161199183 | Rare:23 | ||||
chr1:161314194-161314412 | Common:3; Rare:78; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161766147-161766365 | Common:3; Rare:64 | ||||
chr1:163202899-163203078 | Rare:32 | ||||
chr1:163321764-163322057 | Common:1; Rare:79 | ||||
chr1:165768803-165768938 | Common:1; Rare:63 | ||||
chr1:167935958-167936307 | Common:2; Rare:105 | ||||
chr1:167936556-167936717 | Rare:53 |