| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7440475-7440826 | Rare:71 | ||||
| chr17:7444843-7445111 | Rare:62; Clinvar:1 | ||||
| chr17:7455551-7455826 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:7479545-7479720 | Rare:28 | ||||
| chr17:7484215-7484376 | Common:1; Rare:66 | ||||
| chr17:7484697-7484834 | Rare:57 | ||||
| chr17:7561779-7562008 | Common:2; Rare:63 | ||||
| chr17:7583491-7583876 | Common:1; Rare:152; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:7584073-7584113 | Rare:8 | ||||
| chr17:7627407-7627614 | Common:1; Rare:67 | ||||
| chr17:7650639-7650928 | Common:2; Rare:81 | ||||
| chr17:7687476-7687781 | Rare:52 | ||||
| chr17:7857170-7857300 | Common:1; Rare:73 | ||||
| chr17:7857383-7857413 | Common:1; Rare:8 | ||||
| chr17:7857909-7858278 | Common:1; Rare:140 |