| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:35121483-35121665 | Rare:35 | ||||
| chr17:35142268-35142350 | Rare:26 | ||||
| chr17:35194324-35194433 | Rare:22 | ||||
| chr17:35242901-35243081 | Rare:59 | ||||
| chr17:35373617-35373778 | Common:3; Rare:33 | ||||
| chr17:35578430-35578729 | Common:3; Rare:75; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:35587183-35587597 | Rare:103 | ||||
| chr17:35760770-35760944 | Rare:37 | ||||
| chr17:35795352-35795755 | Rare:109 | ||||
| chr17:35809296-35809580 | Rare:119 | ||||
| chr17:35809734-35809925 | Common:2; Rare:63 | ||||
| chr17:35868834-35868965 | Rare:17 | ||||
| chr17:35930723-35930832 | Rare:38 | ||||
| chr17:35943635-35943781 | Common:2; Rare:28 | ||||
| chr17:36176626-36176718 | Common:2; Rare:5 |