| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:72121979-72122379 | Rare:80 | ||||
| chr17:72122486-72123319 | Common:5; Rare:312; Clinvar:6; Clinvar (benign):7; Clinvar (pathogenic):8 | ||||
| chr17:72151450-72151990 | Common:3; Rare:103 | ||||
| chr17:72219571-72219731 | Rare:34 | ||||
| chr17:72219865-72220091 | Common:2; Rare:49 | ||||
| chr17:72342534-72342958 | Common:4; Rare:230 | ||||
| chr17:72465606-72465864 | Common:2; Rare:45 | ||||
| chr17:72518855-72519651 | Common:9; Rare:275 | ||||
| chr17:72539060-72539480 | Common:8; Rare:82 | ||||
| chr17:72539500-72540000 | Common:4; Rare:96 | ||||
| chr17:72576136-72576597 | Common:6; Rare:128 | ||||
| chr17:72614950-72615330 | Common:2; Rare:83 | ||||
| chr17:73341928-73342328 | Common:3; Rare:128 | ||||
| chr17:73343398-73343576 | Common:1; Rare:28 | ||||
| chr17:73410653-73411418 | Common:19; Rare:302 |