| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:77450453-77450599 | Rare:38 | ||||
| chr17:78130481-78130806 | Common:2; Rare:66 | ||||
| chr17:78187022-78187386 | Common:3; Rare:121 | ||||
| chr17:78692489-78692590 | Common:1; Rare:26 | ||||
| chr17:78840747-78841114 | Common:2; Rare:137 | ||||
| chr17:78979827-78980221 | Common:2; Rare:78 | ||||
| chr17:79009666-79009808 | Common:2; Rare:44; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:79023854-79024179 | Rare:70 | ||||
| chr17:79730838-79731175 | Common:2; Rare:78 | ||||
| chr17:80035843-80036072 | Common:1; Rare:80 | ||||
| chr17:80147003-80147320 | Common:8; Rare:138 | ||||
| chr17:80220309-80220468 | Common:1; Rare:61; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80372819-80373161 | Common:2; Rare:117; Clinvar:1 | ||||
| chr17:80384865-80385124 | Rare:65 | ||||
| chr17:80415115-80415189 | Common:1; Rare:48 |