| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44899367-44899736 | Common:2; Rare:114; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:45051495-45051693 | Common:1; Rare:68 | ||||
| chr17:45060964-45061393 | Common:2; Rare:127 | ||||
| chr17:45096884-45097179 | Common:2; Rare:62 | ||||
| chr17:45104704-45104984 | Common:1; Rare:49 | ||||
| chr17:45132305-45132631 | Common:2; Rare:98 | ||||
| chr17:45148152-45148623 | Common:1; Rare:161 | ||||
| chr17:45161530-45161906 | Common:1; Rare:90 | ||||
| chr17:45431913-45432037 | Common:2; Rare:20 | ||||
| chr17:45487846-45488120 | Common:1; Rare:46 | ||||
| chr17:45490678-45490793 | Common:1; Rare:42 | ||||
| chr17:46193474-46193614 | Common:1; Rare:43 | ||||
| chr17:46818519-46818564 | Rare:17 | ||||
| chr17:46833082-46833283 | Common:2; Rare:38 | ||||
| chr17:46922858-46923187 | Common:4; Rare:91; Clinvar:1; Clinvar (benign):7 |