| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7438020-7438468 | Common:4; Rare:340 | ||||
| chr17:7440193-7441222 | Common:5; Rare:425 | ||||
| chr17:7445260-7446040 | Common:4; Rare:384; Clinvar:3; Clinvar (benign):6 | ||||
| chr17:7455251-7456206 | Common:26; Rare:681; Clinvar:10; Clinvar (benign):23; Clinvar (pathogenic):3 | ||||
| chr17:7478142-7479832 | Common:25; Rare:732 | ||||
| chr17:7483800-7484511 | Common:29; Rare:859 | ||||
| chr17:7484440-7484640 | Common:1; Rare:67 | ||||
| chr17:7484660-7484990 | Rare:610 | ||||
| chr17:7484997-7485439 | Common:10; Rare:201 | ||||
| chr17:7548441-7549119 | Common:12; Rare:415 | ||||
| chr17:7557901-7558456 | Common:5; Rare:145 | ||||
| chr17:7561131-7561396 | Rare:45 | ||||
| chr17:7561620-7562160 | Common:14; Rare:609 | ||||
| chr17:7562293-7562693 | Common:3; Rare:122 | ||||
| chr17:7572378-7572898 | Common:3; Rare:521 |