Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:2593851-2593987 | Common:1; Rare:39; Clinvar:3; Clinvar (benign):3 | ||||
chr17:2711726-2712052 | Common:2; Rare:91 | ||||
chr17:2796204-2796472 | Common:1; Rare:60 | ||||
chr17:3636216-3636779 | Common:8; Rare:160; Clinvar:5; Clinvar (benign):4 | ||||
chr17:3668552-3668876 | Common:2; Rare:129 | ||||
chr17:3723752-3723922 | Common:1; Rare:93 | ||||
chr17:3845922-3846042 | Rare:33 | ||||
chr17:3892952-3893274 | Common:3; Rare:109 | ||||
chr17:3916455-3916628 | Common:1; Rare:38 | ||||
chr17:4142977-4143250 | Rare:95 | ||||
chr17:4143597-4143761 | Common:4; Rare:97 | ||||
chr17:4263937-4264042 | Rare:46 | ||||
chr17:4704110-4704211 | Rare:60 | ||||
chr17:4704301-4704531 | Common:1; Rare:63 | ||||
chr17:4731295-4731484 | Common:2; Rare:55 |