| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43125345-43125685 | Rare:78; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:43170261-43170720 | Common:3; Rare:95 | ||||
| chr17:43171023-43171274 | Common:1; Rare:83 | ||||
| chr17:43211750-43211903 | Common:1; Rare:34 | ||||
| chr17:43778846-43779078 | Rare:55 | ||||
| chr17:44070612-44070947 | Common:3; Rare:116; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44091387-44091686 | Rare:83 | ||||
| chr17:44186658-44187050 | Common:1; Rare:139 | ||||
| chr17:44187169-44187301 | Rare:36 | ||||
| chr17:44198775-44198861 | Rare:25 | ||||
| chr17:44213216-44213375 | Rare:34 | ||||
| chr17:44218225-44218367 | Rare:34 | ||||
| chr17:44219454-44219641 | Rare:68 | ||||
| chr17:44220793-44220924 | Rare:34 | ||||
| chr17:44221211-44221353 | Rare:42 |