Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:46757448-46757918 | Common:1; Rare:80 | ||||
chr16:46758456-46758564 | Rare:18 | ||||
chr16:56617381-56617555 | Common:3; Rare:37 | ||||
chr16:72073003-72073246 | Common:1; Rare:42 | ||||
chr16:72074122-72074236 | Common:1; Rare:28 | ||||
chr16:74368127-74368379 | Common:1; Rare:69 | ||||
chr16:82715907-82716123 | Common:3; Rare:70 | ||||
chr16:84730567-84730614 | Common:2; Rare:10 | ||||
chr17:1774935-1775196 | Common:2; Rare:101; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr17:4999627-4999739 | Common:1; Rare:32 | ||||
chr17:5097294-5097486 | Rare:46 | ||||
chr17:7311071-7311481 | Rare:100 | ||||
chr17:8190063-8190101 | Rare:12 | ||||
chr17:8190130-8190342 | Common:1; Rare:62 | ||||
chr17:8480296-8480479 | Rare:54 |