Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:56971357-56971557 | Common:3; Rare:45; Clinvar (benign):1 | ||||
chr16:58421155-58421326 | Rare:41 | ||||
chr16:64172298-64172441 | Rare:18 | ||||
chr16:64225863-64226142 | Common:1; Rare:79 | ||||
chr16:64317676-64317778 | Common:3; Rare:28 | ||||
chr16:64322016-64322276 | Common:1; Rare:47 | ||||
chr16:72664936-72665175 | Common:1; Rare:76 | ||||
chr16:74297431-74297609 | Common:1; Rare:34 | ||||
chr16:74368127-74368367 | Common:1; Rare:69 | ||||
chr16:81831797-81831999 | Rare:67 | ||||
chr16:83066040-83066333 | Common:4; Rare:85 | ||||
chr16:87779100-87779324 | Common:1; Rare:69 | ||||
chr16:87806513-87806605 | Common:1; Rare:27 | ||||
chr17:2065158-2065234 | Rare:29 | ||||
chr17:6657158-6657349 | Common:5; Rare:26 |