Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:68793049-68793363 | Common:1; Rare:66 | ||||
chr14:69191411-69191582 | Rare:38 | ||||
chr14:69398248-69398389 | Rare:63 | ||||
chr14:69398595-69398723 | Rare:31 | ||||
chr14:73950117-73950323 | Common:5; Rare:79; Clinvar (benign):3 | ||||
chr14:74019248-74019429 | Common:1; Rare:70 | ||||
chr14:74493568-74493771 | Common:3; Rare:76; Clinvar (benign):4 | ||||
chr14:74713070-74713205 | Rare:70 | ||||
chr14:75002783-75002947 | Common:1; Rare:40; Clinvar:2 | ||||
chr14:75660797-75660986 | Rare:48 | ||||
chr14:75661183-75661254 | Common:1; Rare:20 | ||||
chr14:77377040-77377410 | Common:2; Rare:109 | ||||
chr14:77457529-77457844 | Common:1; Rare:101 | ||||
chr14:77708000-77708126 | Rare:62 | ||||
chr14:81220871-81221069 | Common:1; Rare:94 |