| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44899374-44899788 | Common:3; Rare:128; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:44913921-44914103 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:44915130-44915672 | Common:2; Rare:157; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):5 | ||||
| chr17:45051453-45051696 | Common:1; Rare:85 | ||||
| chr17:45060964-45061339 | Common:2; Rare:98 | ||||
| chr17:45132358-45132647 | Common:3; Rare:89 | ||||
| chr17:45148142-45148489 | Common:1; Rare:101 | ||||
| chr17:45161494-45161921 | Common:1; Rare:114 | ||||
| chr17:45490713-45490869 | Rare:53 | ||||
| chr17:45620223-45620376 | Rare:39 | ||||
| chr17:45894247-45894686 | Common:4; Rare:126; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:46225347-46225482 | Common:2; Rare:34 | ||||
| chr17:46818712-46818763 | Rare:11 | ||||
| chr17:46922858-46923187 | Common:4; Rare:91; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47189187-47189568 | Common:1; Rare:102 |