| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:90019373-90019687 | Common:6; Rare:94 | ||||
| chr16:90022552-90022715 | Rare:66 | ||||
| chr17:331389-331659 | Rare:77 | ||||
| chr17:334022-334192 | Rare:45 | ||||
| chr17:336440-336559 | Common:1; Rare:34 | ||||
| chr17:338987-339163 | Common:1; Rare:39 | ||||
| chr17:352760-352842 | Common:1; Rare:20 | ||||
| chr17:386209-386293 | Common:2; Rare:17 | ||||
| chr17:714777-714936 | Common:2; Rare:54 | ||||
| chr17:752143-752354 | Common:2; Rare:86 | ||||
| chr17:752787-752820 | Rare:8 | ||||
| chr17:1279428-1279632 | Common:1; Rare:65 | ||||
| chr17:1467905-1468052 | Rare:66; Clinvar (benign):3 | ||||
| chr17:1485720-1486059 | Common:4; Rare:113 | ||||
| chr17:1491202-1491326 | Common:1; Rare:29 |