Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:76459057-76459261 | Common:1; Rare:75 | ||||
chr9:78236001-78236117 | Rare:38 | ||||
chr9:78296908-78297220 | Common:2; Rare:92; Clinvar (benign):1 | ||||
chr9:83707667-83707708 | Rare:17 | ||||
chr9:83707918-83708292 | Common:3; Rare:119 | ||||
chr9:83921420-83921548 | Common:2; Rare:47 | ||||
chr9:83956668-83956838 | Common:2; Rare:53 | ||||
chr9:83979604-83979730 | Rare:39 | ||||
chr9:83980140-83980359 | Common:2; Rare:75 | ||||
chr9:83980560-83980838 | Common:5; Rare:122 | ||||
chr9:85741895-85742264 | Common:5; Rare:145 | ||||
chr9:85940886-85941234 | Common:3; Rare:118 | ||||
chr9:86282518-86282705 | Common:2; Rare:83 | ||||
chr9:86354287-86354593 | Rare:108 | ||||
chr9:88388214-88388514 | Common:1; Rare:131 |