| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40342027-40342187 | Common:1; Rare:32 | ||||
| chr17:40480353-40480673 | Common:1; Rare:64 | ||||
| chr17:40501237-40501773 | Common:7; Rare:93 | ||||
| chr17:40819612-40820011 | Common:3; Rare:94 | ||||
| chr17:40821959-40822657 | Common:3; Rare:206; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr17:41505685-41505953 | Common:2; Rare:43 | ||||
| chr17:41584970-41585199 | Common:1; Rare:61; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:41586485-41587106 | Common:8; Rare:214; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr17:41624771-41625025 | Rare:68 | ||||
| chr17:41688631-41689061 | Common:3; Rare:170 | ||||
| chr17:41785064-41785393 | Common:2; Rare:77 | ||||
| chr17:41785831-41786216 | Common:2; Rare:68 | ||||
| chr17:41786609-41787163 | Common:3; Rare:132; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:41966579-41966831 | Common:2; Rare:86 | ||||
| chr17:42017382-42017483 | Rare:46 |