| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:63621901-63621970 | Rare:29 | ||||
| chr17:63741765-63741930 | Common:2; Rare:60 | ||||
| chr17:63773435-63773859 | Common:2; Rare:135 | ||||
| chr17:63774052-63774273 | Common:9; Rare:104 | ||||
| chr17:63826997-63827522 | Common:5; Rare:157 | ||||
| chr17:63827906-63828158 | Common:1; Rare:63 | ||||
| chr17:64130033-64130343 | Common:5; Rare:82 | ||||
| chr17:64263208-64263407 | Common:2; Rare:82 | ||||
| chr17:64496989-64497147 | Common:1; Rare:84; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:64503972-64504318 | Common:2; Rare:115 | ||||
| chr17:64662297-64662446 | Common:1; Rare:71 | ||||
| chr17:64919457-64919604 | Common:5; Rare:23 | ||||
| chr17:65056483-65056991 | Common:5; Rare:203 | ||||
| chr17:65137265-65137474 | Common:1; Rare:67 | ||||
| chr17:67245168-67245286 | Rare:40 |