| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44222077-44222414 | Rare:73 | ||||
| chr17:44308435-44308641 | Common:1; Rare:61 | ||||
| chr17:44324777-44324987 | Common:2; Rare:75 | ||||
| chr17:44345030-44345321 | Rare:61; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:44503377-44503710 | Rare:132 | ||||
| chr17:44899375-44899735 | Common:2; Rare:112; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:44915266-44915646 | Common:2; Rare:120; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:45051453-45051691 | Common:1; Rare:84 | ||||
| chr17:45060987-45061339 | Common:2; Rare:93 | ||||
| chr17:45148170-45148478 | Common:1; Rare:93 | ||||
| chr17:45161530-45161789 | Common:1; Rare:58 | ||||
| chr17:45490719-45490867 | Rare:51 | ||||
| chr17:45894247-45894684 | Common:4; Rare:126; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:46922869-46923187 | Common:3; Rare:89; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47189246-47189585 | Rare:86 |