| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:3004900-3005360 | Common:2; Rare:99 | ||||
| chr17:3654609-3655592 | Common:16; Rare:517; Clinvar:13; Clinvar (benign):7; Clinvar (pathogenic):10 | ||||
| chr17:3667036-3667676 | Common:9; Rare:286 | ||||
| chr17:3668050-3668175 | Rare:32 | ||||
| chr17:3959144-3959806 | Common:10; Rare:250 | ||||
| chr17:3965146-3965347 | Rare:86 | ||||
| chr17:3965569-3965687 | Common:2; Rare:28 | ||||
| chr17:3978490-3978820 | Common:1; Rare:54 | ||||
| chr17:4161280-4161530 | Common:4; Rare:121 | ||||
| chr17:4161647-4161873 | Common:1; Rare:75 | ||||
| chr17:4365267-4365519 | Rare:113 | ||||
| chr17:4483523-4484051 | Common:3; Rare:120 | ||||
| chr17:4514320-4514719 | Common:2; Rare:116 | ||||
| chr17:4575690-4576174 | Common:10; Rare:272 | ||||
| chr17:4789585-4789796 | Common:1; Rare:82 |