Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:74431975-74432226 | Common:1; Rare:112 | ||||
chr17:74432553-74432595 | Rare:10 | ||||
chr17:74442843-74443142 | Common:5; Rare:76 | ||||
chr17:74466355-74466706 | Rare:88 | ||||
chr17:74737072-74737275 | Rare:71 | ||||
chr17:74737748-74737798 | Rare:8 | ||||
chr17:74748320-74748751 | Common:6; Rare:150 | ||||
chr17:74776228-74776553 | Common:4; Rare:105 | ||||
chr17:74872600-74872778 | Common:1; Rare:41 | ||||
chr17:74872890-74873048 | Common:2; Rare:67; Clinvar (pathogenic):1 | ||||
chr17:74873135-74873734 | Common:7; Rare:171 | ||||
chr17:74987474-74987653 | Rare:49 | ||||
chr17:75012343-75012815 | Common:2; Rare:114 | ||||
chr17:75012834-75013124 | Common:2; Rare:81 | ||||
chr17:75046350-75046532 | Rare:41 |