| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59106624-59107218 | Common:3; Rare:181; Clinvar:6; Clinvar (benign):4 | ||||
| chr17:59107239-59107428 | Common:2; Rare:35 | ||||
| chr17:59154794-59155036 | Rare:69 | ||||
| chr17:59155054-59155340 | Common:1; Rare:83 | ||||
| chr17:59155542-59155889 | Rare:81 | ||||
| chr17:59209924-59210167 | Common:1; Rare:92 | ||||
| chr17:59210295-59210357 | Rare:17 | ||||
| chr17:59220324-59220736 | Common:4; Rare:124 | ||||
| chr17:59221021-59221202 | Rare:37 | ||||
| chr17:59565460-59565698 | Common:1; Rare:90 | ||||
| chr17:59619066-59619724 | Common:7; Rare:176 | ||||
| chr17:59619744-59620081 | Common:1; Rare:126 | ||||
| chr17:59706568-59706717 | Common:3; Rare:34 | ||||
| chr17:59707143-59707192 | Common:2; Rare:9 | ||||
| chr17:59707240-59707790 | Common:4; Rare:132; Clinvar (benign):6 |