Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:79242522-79242718 | Common:1; Rare:43 | ||||
chr10:79826239-79826498 | Common:3; Rare:82 | ||||
chr10:80207288-80207431 | Common:1; Rare:29 | ||||
chr10:86970916-86971105 | Common:3; Rare:39 | ||||
chr10:86971187-86971268 | Rare:25 | ||||
chr10:87342276-87342410 | Common:3; Rare:43 | ||||
chr10:88939505-88940017 | Common:2; Rare:83; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr10:88944314-88944482 | Rare:26 | ||||
chr10:88946137-88946543 | Common:3; Rare:59 | ||||
chr10:88947489-88947512 | |||||
chr10:88948787-88949117 | Rare:67; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr10:88953600-88953819 | Rare:46 | ||||
chr10:95318418-95318631 | Rare:34 | ||||
chr10:95341283-95341580 | Rare:59 | ||||
chr10:95518916-95518989 | Rare:10 |