| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43778889-43779062 | Rare:41 | ||||
| chr17:43847053-43847176 | Rare:28 | ||||
| chr17:44070631-44070947 | Common:3; Rare:111; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44123599-44123824 | Common:3; Rare:66 | ||||
| chr17:44186608-44187037 | Common:2; Rare:150 | ||||
| chr17:44187161-44187274 | Rare:31 | ||||
| chr17:44198737-44198841 | Rare:35 | ||||
| chr17:44210796-44211066 | Common:1; Rare:81 | ||||
| chr17:44221232-44221451 | Rare:62 | ||||
| chr17:44324750-44324963 | Common:2; Rare:77 | ||||
| chr17:44350277-44350505 | Common:1; Rare:80; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:44503370-44503492 | Rare:49 | ||||
| chr17:44503540-44503580 | Rare:21 | ||||
| chr17:44503584-44503688 | Rare:37 | ||||
| chr17:44899379-44899741 | Common:2; Rare:114; Clinvar:2; Clinvar (benign):1 |