| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:77213183-77213403 | Rare:63 | ||||
| chr17:77319345-77319619 | Common:3; Rare:75; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:77320122-77320323 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:77323123-77323390 | Rare:60 | ||||
| chr17:77324033-77324348 | Common:2; Rare:73 | ||||
| chr17:78187045-78187380 | Common:3; Rare:108 | ||||
| chr17:78359805-78360480 | Common:4; Rare:176 | ||||
| chr17:78378388-78378699 | Common:2; Rare:94 | ||||
| chr17:78379138-78379160 | Rare:3 | ||||
| chr17:78736728-78736971 | Common:1; Rare:49 | ||||
| chr17:78782206-78782575 | Common:9; Rare:122 | ||||
| chr17:78840740-78841114 | Common:2; Rare:141 | ||||
| chr17:78979866-78980201 | Common:2; Rare:66 | ||||
| chr17:79009687-79009924 | Common:9; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:79022728-79022987 | Common:2; Rare:54 |