| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:69141850-69141916 | Rare:16 | ||||
| chr17:69327091-69327334 | Common:2; Rare:81 | ||||
| chr17:70168056-70168302 | Rare:40 | ||||
| chr17:70169177-70169561 | Common:1; Rare:104 | ||||
| chr17:73192817-73193076 | Common:15; Rare:106; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:73232137-73232726 | Common:4; Rare:226 | ||||
| chr17:73644415-73644526 | Rare:27 | ||||
| chr17:74213282-74213583 | Common:4; Rare:63 | ||||
| chr17:74250008-74250331 | Common:4; Rare:80 | ||||
| chr17:74431281-74431408 | Rare:33 | ||||
| chr17:74432001-74432141 | Common:1; Rare:65 | ||||
| chr17:74442819-74443076 | Common:8; Rare:59 | ||||
| chr17:74443469-74443612 | Common:1; Rare:38 | ||||
| chr17:74466287-74466493 | Common:1; Rare:49 | ||||
| chr17:74466556-74466731 | Rare:47 |