| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:51121817-51122004 | Rare:41 | ||||
| chr17:51372707-51372895 | Common:2; Rare:42 | ||||
| chr17:51746251-51746939 | Common:4; Rare:299 | ||||
| chr17:53924633-53924947 | Rare:47 | ||||
| chr17:54372310-54372740 | Common:7; Rare:147 | ||||
| chr17:54956832-54957232 | Common:3; Rare:141 | ||||
| chr17:55238290-55238610 | Common:4; Rare:118 | ||||
| chr17:55601740-55602563 | Common:8; Rare:278 | ||||
| chr17:55606467-55606867 | Common:4; Rare:90 | ||||
| chr17:56010310-56010680 | Common:2; Rare:61 | ||||
| chr17:56325803-56326213 | Common:5; Rare:142 | ||||
| chr17:56359522-56359922 | Common:4; Rare:125 | ||||
| chr17:56594659-56595059 | Common:1; Rare:155; Clinvar (pathogenic):14 | ||||
| chr17:56596640-56597164 | Common:4; Rare:149 | ||||
| chr17:56798894-56799294 | Rare:96 |