Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:79405695-79405901 | Common:1; Rare:62 | ||||
chr13:79406219-79406320 | Common:2; Rare:29 | ||||
chr13:80339279-80339457 | Common:2; Rare:49 | ||||
chr13:93226624-93226890 | Common:2; Rare:50; Clinvar (benign):1 | ||||
chr13:93226960-93227480 | Common:2; Rare:123; Clinvar:7; Clinvar (benign):2 | ||||
chr13:95676894-95677197 | Common:3; Rare:110 | ||||
chr13:96053353-96053482 | Common:1; Rare:54 | ||||
chr13:99200668-99200897 | Common:6; Rare:106 | ||||
chr13:99307397-99307591 | Common:2; Rare:25 | ||||
chr13:100088909-100089117 | Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
chr13:102596785-102597045 | Common:1; Rare:123; Clinvar (benign):1 | ||||
chr13:102773766-102773822 | Rare:24 | ||||
chr13:102845749-102846149 | Common:8; Rare:101; Clinvar:4; Clinvar (benign):4 | ||||
chr13:106567583-106567626 | Rare:12 | ||||
chr13:106567629-106568266 | Rare:183 |