Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:10415120-10415356 | Common:1; Rare:47; Clinvar (benign):1 | ||||
chr17:10415681-10415870 | Common:2; Rare:31 | ||||
chr17:10804053-10804073 | Rare:2 | ||||
chr17:15978066-15978321 | Common:1; Rare:60 | ||||
chr17:16438666-16439018 | Rare:83 | ||||
chr17:16440172-16440251 | Rare:26 | ||||
chr17:18316150-18316469 | Common:1; Rare:96 | ||||
chr17:18572689-18572726 | Rare:5 | ||||
chr17:30576185-30576465 | Common:2; Rare:79 | ||||
chr17:30600311-30600435 | Common:4; Rare:28 | ||||
chr17:30777467-30777631 | Common:1; Rare:43 | ||||
chr17:31008531-31008638 | Common:2; Rare:27 | ||||
chr17:37774479-37774777 | Common:2; Rare:52 | ||||
chr17:37824577-37824759 | Rare:36 | ||||
chr17:39727522-39727738 | Rare:61; Clinvar:2 |