| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:35088478-35088579 | Rare:19 | ||||
| chr17:35089180-35089550 | Common:5; Rare:87 | ||||
| chr17:35119599-35119715 | Rare:44; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr17:35242906-35243076 | Rare:55 | ||||
| chr17:35432440-35432710 | Common:1; Rare:46 | ||||
| chr17:35578525-35578961 | Common:2; Rare:98; Clinvar (benign):1 | ||||
| chr17:35587158-35587364 | Rare:58 | ||||
| chr17:35587420-35587610 | Rare:39 | ||||
| chr17:35731440-35731700 | Rare:65 | ||||
| chr17:35809268-35809534 | Rare:110 | ||||
| chr17:35930709-35930961 | Rare:74 | ||||
| chr17:36064007-36064407 | Common:2; Rare:122 | ||||
| chr17:36486458-36486724 | Common:3; Rare:90 | ||||
| chr17:36534886-36535037 | Common:2; Rare:68 | ||||
| chr17:36535425-36535604 | Common:1; Rare:60 |