| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:5419552-5420234 | Common:6; Rare:228 | ||||
| chr17:5438843-5438972 | Rare:44 | ||||
| chr17:5486157-5486675 | Common:5; Rare:171 | ||||
| chr17:5486801-5486938 | Common:4; Rare:41 | ||||
| chr17:6640640-6641121 | Common:7; Rare:154 | ||||
| chr17:6651539-6651767 | Common:1; Rare:80 | ||||
| chr17:7012301-7012732 | Rare:140 | ||||
| chr17:7012734-7012758 | Rare:10 | ||||
| chr17:7219728-7219971 | Common:3; Rare:99; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:7223307-7223544 | Rare:64 | ||||
| chr17:7223998-7224253 | Rare:96; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):10 | ||||
| chr17:7224467-7224903 | Common:2; Rare:150; Clinvar:12; Clinvar (benign):16; Clinvar (pathogenic):4 | ||||
| chr17:7234462-7234668 | Common:2; Rare:107 | ||||
| chr17:7241602-7241893 | Common:1; Rare:63 | ||||
| chr17:7251916-7252321 | Common:2; Rare:156 |