Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:45149276-45149549 | Common:1; Rare:106 | ||||
chr17:45149761-45149857 | Common:1; Rare:20 | ||||
chr17:45149859-45150074 | Rare:41 | ||||
chr17:45150217-45150356 | Rare:56 | ||||
chr17:45152054-45152099 | Rare:8 | ||||
chr17:45228902-45229265 | Common:3; Rare:67 | ||||
chr17:45247768-45247984 | Common:1; Rare:37 | ||||
chr17:46031711-46031745 | Rare:11; Clinvar:1; Clinvar (benign):1 | ||||
chr17:46036035-46036284 | Common:4; Rare:38 | ||||
chr17:46137107-46137217 | Common:2; Rare:20 | ||||
chr17:46152248-46152318 | Rare:11 | ||||
chr17:47012843-47013085 | Common:1; Rare:46 | ||||
chr17:47067461-47067686 | Common:2; Rare:59 | ||||
chr17:47664044-47664267 | Rare:40 | ||||
chr17:48057130-48057450 | Common:1; Rare:82 |