| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44070642-44070930 | Common:3; Rare:101; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44093479-44093612 | Common:1; Rare:52 | ||||
| chr17:44123588-44123840 | Common:3; Rare:72 | ||||
| chr17:44186629-44187013 | Common:1; Rare:136 | ||||
| chr17:44213262-44213562 | Common:2; Rare:68 | ||||
| chr17:44219006-44219170 | Rare:49 | ||||
| chr17:44220836-44221223 | Common:1; Rare:126 | ||||
| chr17:44221248-44221443 | Rare:54 | ||||
| chr17:44324721-44324976 | Common:4; Rare:95 | ||||
| chr17:44350438-44350733 | Rare:99; Clinvar:6; Clinvar (benign):4 | ||||
| chr17:44352111-44352571 | Common:1; Rare:154; Clinvar:14; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr17:44503341-44503498 | Rare:60 | ||||
| chr17:44503540-44503555 | Rare:6 | ||||
| chr17:44503558-44503709 | Rare:57 | ||||
| chr17:44899375-44899736 | Common:2; Rare:112; Clinvar:1; Clinvar (benign):1 |