| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:51260776-51261200 | Common:9; Rare:340 | ||||
| chr17:54900023-54900423 | Common:1; Rare:64 | ||||
| chr17:54900540-54900971 | Common:2; Rare:155 | ||||
| chr17:54968193-54968593 | Common:1; Rare:212 | ||||
| chr17:54968551-54968881 | Common:11; Rare:312 | ||||
| chr17:55264846-55265028 | Rare:55 | ||||
| chr17:55421786-55422261 | Common:6; Rare:247 | ||||
| chr17:55750837-55751224 | Common:3; Rare:111 | ||||
| chr17:55751247-55751412 | Common:2; Rare:61 | ||||
| chr17:56110840-56111240 | Common:2; Rare:88 | ||||
| chr17:56173990-56174340 | Rare:61 | ||||
| chr17:56593039-56593341 | Rare:66 | ||||
| chr17:56833190-56833590 | Common:1; Rare:153 | ||||
| chr17:56833748-56834277 | Common:14; Rare:421 | ||||
| chr17:56834515-56834915 | Common:2; Rare:173; Clinvar (benign):1; Clinvar (pathogenic):1 |