Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:88943725-88943918 | Common:1; Rare:52; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr10:91807502-91807691 | Rare:38 | ||||
chr10:95322405-95322577 | Common:2; Rare:19 | ||||
chr10:95416526-95416828 | Rare:49 | ||||
chr10:95437786-95437936 | Common:1; Rare:21 | ||||
chr10:95501836-95501926 | Rare:14 | ||||
chr10:95502833-95503213 | Common:3; Rare:63 | ||||
chr10:95503248-95503342 | Rare:13 | ||||
chr10:95506376-95506686 | Common:2; Rare:42 | ||||
chr10:95518899-95519216 | Common:1; Rare:44 | ||||
chr10:95559659-95559803 | Common:1; Rare:38 | ||||
chr10:95605153-95605420 | Common:1; Rare:53 | ||||
chr10:99232569-99232728 | Rare:43 | ||||
chr10:99234300-99234447 | Rare:31 | ||||
chr10:100373420-100373521 | Rare:16 |