| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4967740-4968117 | Common:1; Rare:131 | ||||
| chr17:4987603-4987753 | Common:1; Rare:60 | ||||
| chr17:5191832-5192096 | Common:2; Rare:85 | ||||
| chr17:5234784-5234946 | Rare:43 | ||||
| chr17:5419565-5419890 | Common:4; Rare:116 | ||||
| chr17:5420121-5420272 | Rare:64 | ||||
| chr17:5438843-5439002 | Rare:52 | ||||
| chr17:5486150-5486616 | Common:5; Rare:158 | ||||
| chr17:5486801-5486933 | Common:4; Rare:40 | ||||
| chr17:6556402-6556732 | Common:2; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:6640646-6640867 | Common:2; Rare:51 | ||||
| chr17:6640946-6641226 | Common:4; Rare:120 | ||||
| chr17:6651491-6651774 | Common:1; Rare:97 | ||||
| chr17:6995935-6996108 | Rare:37 | ||||
| chr17:7012317-7012745 | Rare:137 |