Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:76141241-76141494 | Common:1; Rare:63 | ||||
chr17:76353612-76353934 | Common:2; Rare:125 | ||||
chr17:76501372-76501566 | Rare:66; Clinvar (benign):3 | ||||
chr17:76726491-76726903 | Common:5; Rare:154 | ||||
chr17:76737241-76737679 | Common:5; Rare:185 | ||||
chr17:76737883-76738043 | Common:3; Rare:45 | ||||
chr17:77140630-77141038 | Common:3; Rare:145 | ||||
chr17:77287802-77287958 | Rare:19 | ||||
chr17:77319380-77319504 | Common:1; Rare:34 | ||||
chr17:77450688-77450720 | Rare:5 | ||||
chr17:78187052-78187391 | Common:3; Rare:110 | ||||
chr17:78360294-78360469 | Common:2; Rare:46 | ||||
chr17:78378412-78378701 | Common:2; Rare:94 | ||||
chr17:78736738-78737157 | Common:3; Rare:73 | ||||
chr17:78782255-78782572 | Common:9; Rare:105 |