Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:1745327-1745532 | Common:2; Rare:70 | ||||
chr17:1777132-1777261 | Rare:51; Clinvar:1 | ||||
chr17:2335360-2335551 | Common:2; Rare:75 | ||||
chr17:2691616-2691767 | Rare:80 | ||||
chr17:4908403-4908519 | Common:4; Rare:37 | ||||
chr17:4999206-4999257 | Common:1; Rare:6 | ||||
chr17:5020538-5020832 | Common:4; Rare:90; Clinvar (benign):5 | ||||
chr17:7037013-7037070 | Rare:6 | ||||
chr17:7173984-7174268 | Rare:105 | ||||
chr17:7310848-7311122 | Rare:62 | ||||
chr17:7311123-7311481 | Rare:89 | ||||
chr17:8190169-8190261 | Rare:29 | ||||
chr17:8480197-8480404 | Rare:68 | ||||
chr17:8513863-8514000 | Rare:26 | ||||
chr17:10715524-10715743 | Common:1; Rare:56 |