| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4143607-4143740 | Common:4; Rare:75 | ||||
| chr17:4263943-4264042 | Rare:43 | ||||
| chr17:4555317-4555503 | Common:3; Rare:86 | ||||
| chr17:4704107-4704312 | Rare:105 | ||||
| chr17:4710314-4710667 | Common:1; Rare:90 | ||||
| chr17:4731293-4731475 | Common:2; Rare:53 | ||||
| chr17:4786358-4786435 | Rare:19 | ||||
| chr17:4806986-4807192 | Common:4; Rare:66 | ||||
| chr17:4939912-4940111 | Common:1; Rare:67 | ||||
| chr17:4948945-4949124 | Common:1; Rare:61 | ||||
| chr17:4950801-4951147 | Common:1; Rare:77; Clinvar (benign):1 | ||||
| chr17:4967800-4967976 | Rare:67 | ||||
| chr17:5191831-5192116 | Common:2; Rare:89 | ||||
| chr17:5282068-5282287 | Common:10; Rare:110 | ||||
| chr17:5419608-5419876 | Common:3; Rare:91 |