Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:3636630-3636768 | Common:1; Rare:32; Clinvar:3; Clinvar (benign):1 | ||||
chr17:3668539-3668820 | Common:2; Rare:112 | ||||
chr17:3723756-3723941 | Common:1; Rare:106 | ||||
chr17:4263943-4264042 | Rare:43 | ||||
chr17:4555326-4555503 | Common:3; Rare:81 | ||||
chr17:4704110-4704260 | Rare:80 | ||||
chr17:4806953-4807186 | Common:3; Rare:77 | ||||
chr17:4833182-4833456 | Rare:81 | ||||
chr17:4939916-4940081 | Common:1; Rare:55 | ||||
chr17:4948942-4949235 | Common:2; Rare:93 | ||||
chr17:4987414-4987738 | Common:3; Rare:104 | ||||
chr17:5191838-5192047 | Rare:69 | ||||
chr17:5419618-5419994 | Common:6; Rare:109 | ||||
chr17:5420121-5420216 | Rare:39 | ||||
chr17:5486169-5486387 | Common:4; Rare:96 |