| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44187161-44187291 | Rare:34 | ||||
| chr17:44324739-44324959 | Common:3; Rare:81 | ||||
| chr17:44350266-44350577 | Common:1; Rare:108; Clinvar:6; Clinvar (benign):5 | ||||
| chr17:44350686-44351455 | Common:1; Rare:239; Clinvar:12; Clinvar (benign):5; Clinvar (pathogenic):5 | ||||
| chr17:44351708-44352108 | Rare:132; Clinvar:8; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:44352111-44352571 | Common:1; Rare:154; Clinvar:14; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr17:44503366-44503707 | Rare:133 | ||||
| chr17:44899375-44899741 | Common:2; Rare:115; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:45051582-45051688 | Rare:37 | ||||
| chr17:45060993-45061353 | Common:2; Rare:102 | ||||
| chr17:45148159-45148478 | Common:1; Rare:93 | ||||
| chr17:45490693-45490867 | Common:1; Rare:60 | ||||
| chr17:46193467-46193604 | Common:1; Rare:39 | ||||
| chr17:46922869-46923194 | Common:3; Rare:95; Clinvar:2; Clinvar (benign):7 | ||||
| chr17:47188832-47188942 | Rare:14 |