| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:78681010-78681179 | Rare:38 | ||||
| chr17:78782203-78782549 | Common:6; Rare:108 | ||||
| chr17:78840745-78841114 | Common:2; Rare:139 | ||||
| chr17:79009680-79009924 | Common:9; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:79023880-79024101 | Rare:49 | ||||
| chr17:79025368-79025694 | Common:4; Rare:60 | ||||
| chr17:79993708-79993824 | Rare:21 | ||||
| chr17:80035830-80036072 | Common:1; Rare:81 | ||||
| chr17:80036585-80036665 | Common:2; Rare:19; Clinvar (benign):2 | ||||
| chr17:80147117-80147331 | Common:5; Rare:83 | ||||
| chr17:80187694-80187811 | Rare:31 | ||||
| chr17:80220297-80220485 | Common:1; Rare:72; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80363010-80363146 | Rare:43 | ||||
| chr17:80372700-80373001 | Common:1; Rare:84 | ||||
| chr17:80415109-80415197 | Common:1; Rare:59 |