| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42423202-42423554 | Common:1; Rare:88; Clinvar:1 | ||||
| chr17:42458667-42458956 | Common:3; Rare:109 | ||||
| chr17:42520095-42520390 | Common:1; Rare:61 | ||||
| chr17:42536035-42536345 | Common:4; Rare:93; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr17:42536544-42536814 | Common:3; Rare:65; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr17:42541443-42541609 | Common:1; Rare:20 | ||||
| chr17:42552132-42552424 | Common:3; Rare:50 | ||||
| chr17:42561964-42562222 | Common:1; Rare:76 | ||||
| chr17:42562392-42562611 | Common:1; Rare:88; Clinvar (benign):1 | ||||
| chr17:42562754-42562878 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:42566922-42567288 | Common:4; Rare:124 | ||||
| chr17:42567450-42567640 | Common:1; Rare:58 | ||||
| chr17:42577293-42577336 | Common:1; Rare:16; Clinvar (benign):1 | ||||
| chr17:42577621-42577917 | Common:1; Rare:149 | ||||
| chr17:42608842-42609126 | Common:2; Rare:76 |