Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:48107427-48107599 | Common:3; Rare:41 | ||||
chr17:48544477-48544503 | Rare:7 | ||||
chr17:48544558-48544651 | Rare:47 | ||||
chr17:48944758-48944859 | Rare:37 | ||||
chr17:49210526-49210727 | Rare:35 | ||||
chr17:49414845-49415114 | Common:1; Rare:65 | ||||
chr17:49578572-49578622 | Rare:9 | ||||
chr17:49677971-49678376 | Rare:104 | ||||
chr17:49788462-49788753 | Common:1; Rare:95 | ||||
chr17:50056137-50056618 | Common:1; Rare:120 | ||||
chr17:50188901-50189258 | Rare:90; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr17:50196161-50196434 | Common:2; Rare:80; Clinvar:2; Clinvar (benign):2 | ||||
chr17:50866312-50866560 | Common:3; Rare:83 | ||||
chr17:51079496-51079650 | Common:1; Rare:37 | ||||
chr17:51120396-51120551 | Common:1; Rare:24 |