Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:66654438-66654567 | Rare:49 | ||||
chr7:66844872-66845065 | Common:2; Rare:79 | ||||
chr7:67302402-67302686 | Common:5; Rare:91 | ||||
chr7:72836602-72836869 | Common:1; Rare:44 | ||||
chr7:73005826-73006164 | Rare:37 | ||||
chr7:73769565-73769629 | Rare:25 | ||||
chr7:74890532-74890836 | Common:2; Rare:102 | ||||
chr7:75916852-75916865 | |||||
chr7:76064685-76064922 | Common:1; Rare:86 | ||||
chr7:79454809-79454996 | Rare:31 | ||||
chr7:87419386-87419421 | Rare:4 | ||||
chr7:95396931-95397056 | Common:1; Rare:20 | ||||
chr7:95406123-95406394 | Common:1; Rare:63; Clinvar (benign):1 | ||||
chr7:95410045-95410334 | Common:4; Rare:49 | ||||
chr7:95441132-95441277 | Common:2; Rare:27 |