| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:21098904-21099597 | Common:13; Rare:490 | ||||
| chr17:21275831-21275971 | Common:2; Rare:99 | ||||
| chr17:21411050-21411350 | Rare:19 | ||||
| chr17:27332770-27333355 | Common:5; Rare:157 | ||||
| chr17:27353741-27354032 | Common:1; Rare:144 | ||||
| chr17:27540320-27540690 | Common:4; Rare:102 | ||||
| chr17:28737960-28738310 | Common:2; Rare:187; Clinvar:9; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:29133430-29134110 | Common:2; Rare:223 | ||||
| chr17:29155330-29155780 | Common:3; Rare:111 | ||||
| chr17:29178120-29178520 | Common:2; Rare:113 | ||||
| chr17:29179441-29179627 | Common:2; Rare:64 | ||||
| chr17:30600297-30600509 | Common:8; Rare:75 | ||||
| chr17:30600580-30600900 | Common:2; Rare:121 | ||||
| chr17:30731365-30731754 | Common:9; Rare:240 | ||||
| chr17:31549511-31549741 | Common:4; Rare:97 |