| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40140150-40140551 | Common:5; Rare:188 | ||||
| chr17:40318085-40318293 | Common:1; Rare:46 | ||||
| chr17:40342038-40342399 | Common:1; Rare:79 | ||||
| chr17:40417860-40418166 | Rare:89 | ||||
| chr17:41505056-41505424 | Common:4; Rare:130; Clinvar:2; Clinvar (benign):7 | ||||
| chr17:41505736-41505940 | Common:2; Rare:35 | ||||
| chr17:41586870-41587140 | Common:1; Rare:61 | ||||
| chr17:41812829-41813022 | Rare:50; Clinvar:2 | ||||
| chr17:41966614-41966815 | Common:1; Rare:71 | ||||
| chr17:42154941-42155251 | Common:3; Rare:80 | ||||
| chr17:42423054-42423462 | Common:1; Rare:115; Clinvar:2 | ||||
| chr17:42458749-42458909 | Common:1; Rare:62 | ||||
| chr17:42577655-42577844 | Rare:89 | ||||
| chr17:42609333-42609705 | Common:8; Rare:150; Clinvar (benign):1 | ||||
| chr17:42761019-42761254 | Rare:66 |