Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:67360263-67360368 | Common:1; Rare:33 | ||||
chr14:68978259-68978402 | Common:2; Rare:42 | ||||
chr14:69398256-69398426 | Common:1; Rare:64 | ||||
chr14:69398573-69398725 | Rare:36 | ||||
chr14:69611456-69611759 | Common:1; Rare:101 | ||||
chr14:70416977-70417138 | Rare:49 | ||||
chr14:73787166-73787371 | Common:2; Rare:76 | ||||
chr14:73950130-73950330 | Common:4; Rare:85; Clinvar (benign):2 | ||||
chr14:74019259-74019432 | Common:1; Rare:69 | ||||
chr14:74493570-74493784 | Common:3; Rare:80; Clinvar (benign):4 | ||||
chr14:74494105-74494330 | Rare:84; Clinvar (benign):2 | ||||
chr14:74713070-74713207 | Rare:71 | ||||
chr14:75069484-75069677 | Common:1; Rare:45 | ||||
chr14:75127008-75127132 | Rare:42 | ||||
chr14:75660875-75661333 | Common:4; Rare:104 |