Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:752146-752347 | Common:2; Rare:78 | ||||
chr17:1516588-1516949 | Common:1; Rare:123 | ||||
chr17:1716204-1716518 | Common:2; Rare:93 | ||||
chr17:1829768-1830085 | Common:8; Rare:136 | ||||
chr17:2303781-2303987 | Common:2; Rare:75 | ||||
chr17:2511844-2512021 | Common:2; Rare:54 | ||||
chr17:3636241-3636479 | Common:4; Rare:63; Clinvar (benign):1 | ||||
chr17:3668546-3668828 | Common:2; Rare:110 | ||||
chr17:3723776-3723938 | Common:1; Rare:92 | ||||
chr17:4143011-4143244 | Rare:76 | ||||
chr17:4143617-4143727 | Common:4; Rare:61 | ||||
chr17:4263943-4264042 | Rare:43 | ||||
chr17:4555320-4555525 | Common:3; Rare:96 | ||||
chr17:4704117-4704211 | Rare:55 | ||||
chr17:4807008-4807192 | Common:4; Rare:62 |