Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:1562722-1562946 | Common:3; Rare:82 | ||||
chr17:1653542-1653851 | Common:3; Rare:63; Clinvar:1; Clinvar (benign):2 | ||||
chr17:1684734-1685067 | Common:2; Rare:116; Clinvar:7; Clinvar (benign):1 | ||||
chr17:1710310-1710516 | Rare:59 | ||||
chr17:1716201-1716518 | Common:2; Rare:94 | ||||
chr17:1724652-1724737 | Common:1; Rare:34 | ||||
chr17:1761972-1762146 | Common:2; Rare:36; Clinvar (benign):2 | ||||
chr17:1762689-1762829 | Common:2; Rare:36 | ||||
chr17:1829769-1830094 | Common:8; Rare:135 | ||||
chr17:2303345-2303683 | Rare:120 | ||||
chr17:2303708-2304010 | Common:2; Rare:113 | ||||
chr17:2335828-2335950 | Rare:35 | ||||
chr17:2336326-2336563 | Rare:104 | ||||
chr17:2337316-2337523 | Rare:62 | ||||
chr17:2400965-2401268 | Rare:88 |