| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8299068-8299297 | Common:3; Rare:42 | ||||
| chr17:8377647-8377899 | Common:1; Rare:50 | ||||
| chr17:8631321-8631523 | Common:1; Rare:67 | ||||
| chr17:8650836-8650957 | Common:1; Rare:21 | ||||
| chr17:9353946-9354262 | Common:1; Rare:55 | ||||
| chr17:11110119-11110195 | Rare:18 | ||||
| chr17:11944708-11944835 | Rare:25 | ||||
| chr17:12138793-12138860 | Rare:11 | ||||
| chr17:14030532-14030817 | Common:5; Rare:71 | ||||
| chr17:14705085-14705110 | Rare:6 | ||||
| chr17:14776750-14777155 | Common:3; Rare:79 | ||||
| chr17:15443172-15443437 | Common:3; Rare:47 | ||||
| chr17:15972539-15972738 | Common:3; Rare:35 | ||||
| chr17:15981027-15981053 | Rare:6 | ||||
| chr17:16006478-16006769 | Common:1; Rare:64; Clinvar:3; Clinvar (pathogenic):2 |