Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:89884634-89884678 | Rare:21 | ||||
chr16:89972478-89972661 | Common:1; Rare:66 | ||||
chr16:90008889-90009267 | Common:5; Rare:108 | ||||
chr16:90019400-90019643 | Common:4; Rare:74 | ||||
chr17:751533-751788 | Rare:64 | ||||
chr17:752163-752357 | Common:2; Rare:78 | ||||
chr17:1516588-1516952 | Common:1; Rare:126 | ||||
chr17:1628789-1628891 | Rare:39 | ||||
chr17:1829786-1830126 | Common:9; Rare:141 | ||||
chr17:2303734-2303978 | Common:2; Rare:92 | ||||
chr17:2336420-2336510 | Rare:33 | ||||
chr17:2392642-2392916 | Common:6; Rare:131 | ||||
chr17:2401041-2401387 | Common:1; Rare:112 | ||||
chr17:2796204-2796472 | Common:1; Rare:60 | ||||
chr17:3636269-3636479 | Common:4; Rare:42; Clinvar (benign):1 |