| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:65561024-65561230 | Rare:81 | ||||
| chr17:65561452-65561654 | Common:2; Rare:77; Clinvar:7; Clinvar (benign):1 | ||||
| chr17:65561996-65562207 | Common:1; Rare:56 | ||||
| chr17:66191659-66191790 | Rare:19 | ||||
| chr17:66192040-66192387 | Common:3; Rare:108 | ||||
| chr17:66302199-66302676 | Common:5; Rare:161 | ||||
| chr17:66302914-66302934 | Rare:2 | ||||
| chr17:66303122-66303197 | Rare:15 | ||||
| chr17:66303347-66303476 | Common:1; Rare:30 | ||||
| chr17:66964342-66964536 | Common:5; Rare:49 | ||||
| chr17:66964623-66964748 | Rare:36 | ||||
| chr17:66965002-66965241 | Common:16; Rare:95 | ||||
| chr17:66965341-66965363 | Rare:5 | ||||
| chr17:67245095-67245522 | Rare:137 | ||||
| chr17:67245651-67246172 | Common:5; Rare:144 |