| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:78121099-78121384 | Common:4; Rare:51 | ||||
| chr17:78125202-78125466 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:78126880-78127176 | Rare:63 | ||||
| chr17:78127287-78127428 | Common:1; Rare:34 | ||||
| chr17:78128658-78128864 | Common:7; Rare:55 | ||||
| chr17:78130616-78130835 | Rare:43 | ||||
| chr17:78187029-78187382 | Common:3; Rare:116 | ||||
| chr17:78378589-78378719 | Common:1; Rare:55 | ||||
| chr17:78403271-78403626 | Common:3; Rare:75 | ||||
| chr17:78678954-78679148 | Rare:44 | ||||
| chr17:78782216-78782554 | Common:9; Rare:107 | ||||
| chr17:78840736-78841047 | Common:2; Rare:113 | ||||
| chr17:78977198-78977498 | Common:3; Rare:60 | ||||
| chr17:78979827-78980201 | Common:2; Rare:76 | ||||
| chr17:78995088-78995489 | Common:3; Rare:110; Clinvar:2; Clinvar (pathogenic):2 |