| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:78840747-78841114 | Common:2; Rare:137 | ||||
| chr17:78979866-78980201 | Common:2; Rare:66 | ||||
| chr17:80035843-80036037 | Common:1; Rare:68 | ||||
| chr17:80146958-80147412 | Common:10; Rare:202 | ||||
| chr17:80192060-80192198 | Rare:26 | ||||
| chr17:80220309-80220453 | Rare:57; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80415105-80415197 | Common:1; Rare:64 | ||||
| chr17:80415387-80415492 | Common:4; Rare:40 | ||||
| chr17:80991777-80991930 | Common:1; Rare:58 | ||||
| chr17:81087288-81087569 | Common:1; Rare:76 | ||||
| chr17:81097411-81097631 | Rare:81 | ||||
| chr17:81239029-81239317 | Common:2; Rare:96 | ||||
| chr17:81295266-81295373 | Common:1; Rare:21 | ||||
| chr17:81511891-81512403 | Common:3; Rare:249; Clinvar:8; Clinvar (benign):32; Clinvar (pathogenic):2 | ||||
| chr17:81512725-81513159 | Common:7; Rare:216; Clinvar (benign):14 |