Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:41688661-41689043 | Common:3; Rare:159 | ||||
chr17:41812593-41813016 | Common:3; Rare:89; Clinvar:5 | ||||
chr17:42017388-42017484 | Rare:42 | ||||
chr17:42423113-42423341 | Rare:61; Clinvar:2 | ||||
chr17:42566913-42567156 | Common:3; Rare:87 | ||||
chr17:42577648-42577849 | Rare:97 | ||||
chr17:42609265-42609731 | Common:9; Rare:195; Clinvar (benign):2 | ||||
chr17:42682423-42682537 | Rare:22 | ||||
chr17:42798654-42798769 | Rare:37 | ||||
chr17:42964422-42964524 | Rare:50 | ||||
chr17:42980423-42980594 | Common:1; Rare:64 | ||||
chr17:42998358-42998468 | Common:3; Rare:33 | ||||
chr17:42998582-42998812 | Rare:53 | ||||
chr17:43125343-43125685 | Rare:78; Clinvar:3; Clinvar (benign):2 | ||||
chr17:43170195-43170431 | Common:1; Rare:54 |