Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:89972455-89972580 | Common:1; Rare:40 | ||||
chr17:714763-714901 | Common:2; Rare:45 | ||||
chr17:1516570-1516937 | Common:1; Rare:128 | ||||
chr17:1716172-1716538 | Common:3; Rare:116 | ||||
chr17:1829786-1830082 | Common:8; Rare:126 | ||||
chr17:2303514-2303635 | Rare:42 | ||||
chr17:2303736-2303987 | Common:2; Rare:94 | ||||
chr17:2336420-2336572 | Rare:62 | ||||
chr17:3636244-3636546 | Common:5; Rare:82; Clinvar (benign):2 | ||||
chr17:3668503-3668820 | Common:3; Rare:128 | ||||
chr17:3723765-3723929 | Common:1; Rare:93 | ||||
chr17:4142943-4143234 | Common:3; Rare:102 | ||||
chr17:4263934-4264045 | Rare:47 | ||||
chr17:4555311-4555542 | Common:3; Rare:106 | ||||
chr17:4731296-4731481 | Common:2; Rare:54 |