| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28335404-28335852 | Common:1; Rare:102 | ||||
| chr17:28357426-28357781 | Common:6; Rare:169; Clinvar (pathogenic):2 | ||||
| chr17:28371314-28371799 | Common:6; Rare:94 | ||||
| chr17:28384467-28384916 | Rare:133 | ||||
| chr17:28385136-28385243 | Rare:39 | ||||
| chr17:28405744-28405910 | Rare:37 | ||||
| chr17:28406051-28406320 | Rare:67; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr17:28547732-28547921 | Rare:58; Clinvar:3 | ||||
| chr17:28549759-28550021 | Common:1; Rare:52 | ||||
| chr17:28571462-28571763 | Rare:91 | ||||
| chr17:28576840-28577084 | Common:2; Rare:66 | ||||
| chr17:28598933-28599260 | Common:3; Rare:107 | ||||
| chr17:28599567-28599782 | Rare:43 | ||||
| chr17:28645027-28645390 | Common:1; Rare:149 | ||||
| chr17:28661621-28661729 | Rare:32 |