Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:75844479-75844611 | Common:3; Rare:30; Clinvar:4; Clinvar (benign):2 | ||||
chr17:75875992-75876327 | Rare:83 | ||||
chr17:75979126-75979279 | Rare:40; Clinvar:4 | ||||
chr17:75979420-75979611 | Rare:58 | ||||
chr17:76072385-76072533 | Common:6; Rare:112 | ||||
chr17:76103711-76103898 | Common:5; Rare:61 | ||||
chr17:76726413-76726914 | Common:5; Rare:190 | ||||
chr17:76737372-76737691 | Common:3; Rare:92 | ||||
chr17:78130655-78130850 | Rare:35 | ||||
chr17:78187018-78187379 | Common:3; Rare:123 | ||||
chr17:78736749-78736971 | Common:1; Rare:40 | ||||
chr17:78782196-78782583 | Common:9; Rare:126 | ||||
chr17:78840736-78841115 | Common:2; Rare:144 | ||||
chr17:80036581-80036695 | Common:2; Rare:32; Clinvar (benign):2 | ||||
chr17:80147141-80147377 | Common:6; Rare:83 |