| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:46225349-46225471 | Common:1; Rare:32 | ||||
| chr17:46922869-46923204 | Common:4; Rare:102; Clinvar:3; Clinvar (benign):8 | ||||
| chr17:47189102-47189619 | Common:1; Rare:138 | ||||
| chr17:47208864-47209557 | Rare:146; Clinvar:2 | ||||
| chr17:47323894-47323992 | Common:1; Rare:28 | ||||
| chr17:47530963-47531296 | Rare:90 | ||||
| chr17:47649518-47649987 | Common:1; Rare:171 | ||||
| chr17:47831501-47831588 | Rare:30 | ||||
| chr17:47941354-47941732 | Rare:102; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:47970804-47971152 | Common:1; Rare:77 | ||||
| chr17:48037173-48037460 | Common:2; Rare:67 | ||||
| chr17:48048057-48048409 | Rare:95 | ||||
| chr17:48048599-48048862 | Common:4; Rare:41 | ||||
| chr17:48101280-48101568 | Common:3; Rare:82 | ||||
| chr17:48107661-48107817 | Common:1; Rare:39 |