| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:37744367-37744696 | Common:1; Rare:123; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr17:37744845-37744908 | Rare:15; Clinvar:1 | ||||
| chr17:37745013-37745417 | Rare:98; Clinvar (benign):2 | ||||
| chr17:37745642-37745703 | Rare:9 | ||||
| chr17:38296871-38297243 | Common:6; Rare:123 | ||||
| chr17:38351592-38352082 | Common:4; Rare:164 | ||||
| chr17:38352125-38352278 | Rare:26 | ||||
| chr17:38419127-38419295 | Common:1; Rare:42 | ||||
| chr17:38453505-38453748 | Common:2; Rare:47 | ||||
| chr17:38454055-38454110 | Rare:6 | ||||
| chr17:38559464-38559649 | Rare:55 | ||||
| chr17:38572975-38573052 | Rare:22 | ||||
| chr17:38605878-38606258 | Common:2; Rare:117 | ||||
| chr17:38606426-38606791 | Common:3; Rare:84 | ||||
| chr17:38674870-38675196 | Common:3; Rare:85 |