| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44070612-44070930 | Common:3; Rare:108; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44123594-44123863 | Common:3; Rare:80 | ||||
| chr17:44186695-44187009 | Rare:104 | ||||
| chr17:44187142-44187283 | Rare:38 | ||||
| chr17:44221211-44221374 | Rare:47 | ||||
| chr17:44308432-44308635 | Common:1; Rare:59 | ||||
| chr17:44324760-44325013 | Common:2; Rare:91 | ||||
| chr17:44345025-44345321 | Rare:63; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:44503366-44503720 | Rare:137 | ||||
| chr17:44899375-44899750 | Common:2; Rare:118; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:44911469-44911756 | Common:5; Rare:97; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:44913662-44913842 | Rare:71; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr17:44915026-44915664 | Common:2; Rare:192; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):5 | ||||
| chr17:45051571-45051688 | Rare:42 | ||||
| chr17:45060992-45061332 | Common:2; Rare:89 |