Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:1829832-1830016 | Common:4; Rare:77 | ||||
chr17:2303728-2303973 | Common:2; Rare:89 | ||||
chr17:2336430-2336550 | Rare:46 | ||||
chr17:2511820-2511926 | Common:2; Rare:27 | ||||
chr17:3636246-3636517 | Common:4; Rare:75; Clinvar (benign):1 | ||||
chr17:3668546-3668849 | Common:2; Rare:122 | ||||
chr17:3723802-3723917 | Rare:63 | ||||
chr17:4143011-4143225 | Rare:71 | ||||
chr17:4263948-4264072 | Rare:51 | ||||
chr17:4704116-4704260 | Rare:76 | ||||
chr17:4739830-4739990 | Rare:31 | ||||
chr17:4806982-4807192 | Common:4; Rare:70 | ||||
chr17:4833246-4833503 | Rare:75 | ||||
chr17:4939916-4940130 | Common:2; Rare:72 | ||||
chr17:4948482-4948654 | Common:2; Rare:73 |