| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4896334-4896546 | Rare:89 | ||||
| chr17:4899519-4899717 | Common:2; Rare:67; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr17:4939916-4940761 | Common:5; Rare:232 | ||||
| chr17:4947900-4948046 | Rare:42 | ||||
| chr17:4948945-4949084 | Common:1; Rare:47 | ||||
| chr17:4967489-4967611 | Common:2; Rare:39 | ||||
| chr17:4967762-4967909 | Rare:62 | ||||
| chr17:4986337-4986479 | Common:2; Rare:26 | ||||
| chr17:4987431-4987753 | Common:3; Rare:107 | ||||
| chr17:4997472-4997670 | Common:1; Rare:74 | ||||
| chr17:4997884-4998075 | Common:1; Rare:74 | ||||
| chr17:5014074-5014211 | Common:2; Rare:23 | ||||
| chr17:5078141-5078547 | Common:4; Rare:100 | ||||
| chr17:5115935-5116226 | Common:4; Rare:83 | ||||
| chr17:5116354-5116560 | Common:2; Rare:45 |