| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:79993480-79993954 | Common:2; Rare:169 | ||||
| chr17:80035726-80036126 | Common:3; Rare:179 | ||||
| chr17:80036410-80036770 | Common:6; Rare:174; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:80101290-80101690 | Common:19; Rare:580; Clinvar:1; Clinvar (benign):17 | ||||
| chr17:80146958-80147467 | Common:39; Rare:776 | ||||
| chr17:80147497-80147897 | Rare:105 | ||||
| chr17:80219420-80219820 | Common:2; Rare:101 | ||||
| chr17:80220203-80220603 | Common:6; Rare:373; Clinvar:6; Clinvar (pathogenic):4 | ||||
| chr17:80260040-80260926 | Common:59; Rare:579 | ||||
| chr17:80260835-80261235 | Common:1; Rare:123 | ||||
| chr17:80414923-80415323 | Common:7; Rare:643 | ||||
| chr17:80415270-80415680 | Common:27; Rare:531 | ||||
| chr17:80544545-80545880 | Common:40; Rare:1116 | ||||
| chr17:80991572-80991972 | Common:9; Rare:431 | ||||
| chr17:81034746-81035166 | Common:10; Rare:635 |