Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:76671688-76671988 | Common:2; Rare:72 | ||||
chr17:77441797-77441895 | Common:1; Rare:20 | ||||
chr17:77445476-77445640 | Common:1; Rare:48 | ||||
chr17:77492624-77493075 | Common:2; Rare:111; Clinvar (benign):2 | ||||
chr17:77888002-77888246 | Common:1; Rare:66 | ||||
chr17:78140590-78140797 | Common:2; Rare:66 | ||||
chr17:78154987-78155026 | Rare:6 | ||||
chr17:78173478-78173699 | Common:3; Rare:40 | ||||
chr17:78676306-78676480 | Common:1; Rare:44 | ||||
chr17:78779817-78779946 | Rare:20 | ||||
chr17:78779961-78780020 | Rare:11 | ||||
chr17:78889014-78889195 | Common:2; Rare:41 | ||||
chr17:79942865-79943095 | Common:3; Rare:51 | ||||
chr17:81509878-81510051 | Common:1; Rare:86 | ||||
chr17:82297484-82297700 | Rare:57 |