| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:32837355-32837570 | Common:2; Rare:33 | ||||
| chr17:32856150-32856216 | Common:2; Rare:15 | ||||
| chr17:32869955-32869986 | Rare:5 | ||||
| chr17:32876230-32876605 | Common:2; Rare:89 | ||||
| chr17:32929342-32929419 | Rare:22 | ||||
| chr17:34252512-34252861 | Common:2; Rare:71; Clinvar (pathogenic):1 | ||||
| chr17:34252922-34253132 | Common:2; Rare:22 | ||||
| chr17:35050102-35050326 | Rare:24 | ||||
| chr17:35065223-35065287 | Common:1; Rare:12 | ||||
| chr17:35089866-35089965 | Common:1; Rare:17 | ||||
| chr17:35151209-35151297 | Rare:22 | ||||
| chr17:35243789-35243995 | Rare:31 | ||||
| chr17:35356707-35356775 | Rare:11 | ||||
| chr17:35356807-35357124 | Common:6; Rare:54 | ||||
| chr17:35372811-35372862 | Common:1; Rare:10 |