Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:79405792-79405882 | Rare:35 | ||||
chr13:79406198-79406306 | Common:2; Rare:31 | ||||
chr13:95301417-95301541 | Rare:35 | ||||
chr13:95676937-95677176 | Common:3; Rare:76 | ||||
chr13:96053358-96053546 | Common:2; Rare:80 | ||||
chr13:97222207-97222401 | Rare:32 | ||||
chr13:98978020-98978179 | Common:1; Rare:34 | ||||
chr13:99200668-99200894 | Common:6; Rare:104 | ||||
chr13:99606531-99606690 | Common:4; Rare:42 | ||||
chr13:100088920-100089117 | Rare:70; Clinvar:1; Clinvar (benign):2 | ||||
chr13:100674778-100675060 | Common:3; Rare:115 | ||||
chr13:102596785-102597028 | Common:1; Rare:113 | ||||
chr13:102773708-102773849 | Rare:62 | ||||
chr13:102798950-102799124 | Common:1; Rare:37 | ||||
chr13:106568053-106568261 | Rare:61 |