| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45161388-45161641 | Rare:76 | ||||
| chr17:45262071-45262204 | Common:1; Rare:15 | ||||
| chr17:45316606-45316642 | Rare:10 | ||||
| chr17:45316930-45317362 | Common:5; Rare:109 | ||||
| chr17:45317398-45317626 | Rare:55 | ||||
| chr17:45490693-45490951 | Common:7; Rare:82 | ||||
| chr17:45784033-45784244 | Common:1; Rare:49 | ||||
| chr17:45894194-45894325 | Common:2; Rare:45 | ||||
| chr17:45894329-45894572 | Common:2; Rare:69; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:46192523-46192599 | Common:3; Rare:11; Clinvar (benign):3 | ||||
| chr17:46192709-46193024 | Common:3; Rare:78; Clinvar (benign):4 | ||||
| chr17:46193041-46193129 | Common:1; Rare:17 | ||||
| chr17:46193230-46193832 | Common:9; Rare:154 | ||||
| chr17:46193833-46193928 | Rare:28 | ||||
| chr17:46193943-46194155 | Common:5; Rare:38 |