Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:996787-997164 | Common:2; Rare:115 | ||||
chr17:1078950-1079141 | Rare:50 | ||||
chr17:1083613-1083726 | Rare:32 | ||||
chr17:1399446-1399759 | Common:2; Rare:97 | ||||
chr17:1400046-1400380 | Common:3; Rare:141 | ||||
chr17:1516561-1517008 | Common:2; Rare:156 | ||||
chr17:1628266-1628539 | Common:1; Rare:81 | ||||
chr17:1628793-1628991 | Rare:69 | ||||
chr17:1673106-1673413 | Common:2; Rare:72; Clinvar:2 | ||||
chr17:1684406-1684495 | Common:1; Rare:40 | ||||
chr17:1684764-1685082 | Common:2; Rare:111; Clinvar:7; Clinvar (benign):1 | ||||
chr17:1716204-1716513 | Common:2; Rare:92 | ||||
chr17:1829770-1830082 | Common:8; Rare:133 | ||||
chr17:2303456-2303575 | Rare:42 | ||||
chr17:2303716-2304001 | Common:2; Rare:109 |