| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44092475-44092772 | Common:1; Rare:77 | ||||
| chr17:44093179-44093495 | Common:1; Rare:104 | ||||
| chr17:44111225-44111414 | Rare:56 | ||||
| chr17:44123514-44123840 | Common:3; Rare:96 | ||||
| chr17:44186608-44187002 | Common:2; Rare:143 | ||||
| chr17:44187044-44187294 | Rare:58 | ||||
| chr17:44220810-44221195 | Common:1; Rare:132 | ||||
| chr17:44221269-44221309 | Rare:13 | ||||
| chr17:44308421-44308598 | Common:1; Rare:57 | ||||
| chr17:44324728-44324963 | Common:3; Rare:85 | ||||
| chr17:44350437-44350794 | Rare:124; Clinvar:8; Clinvar (benign):4 | ||||
| chr17:44351789-44352108 | Rare:98; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:44352111-44352459 | Rare:118; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr17:44503326-44503475 | Rare:54 | ||||
| chr17:44503540-44503638 | Rare:49 |