| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59964706-59965044 | Common:2; Rare:101 | ||||
| chr17:60078917-60078974 | Common:4; Rare:30 | ||||
| chr17:60526211-60526541 | Common:2; Rare:87 | ||||
| chr17:63773511-63773858 | Common:2; Rare:115 | ||||
| chr17:63827057-63827732 | Common:7; Rare:195 | ||||
| chr17:64130010-64130362 | Common:6; Rare:91 | ||||
| chr17:64390568-64390876 | Common:1; Rare:49 | ||||
| chr17:64506075-64506785 | Common:8; Rare:296 | ||||
| chr17:65056582-65056956 | Common:4; Rare:154 | ||||
| chr17:67366528-67366682 | Rare:54 | ||||
| chr17:67717629-67717945 | Common:3; Rare:105 | ||||
| chr17:68247866-68248114 | Common:5; Rare:107 | ||||
| chr17:68291172-68291520 | Common:1; Rare:100 | ||||
| chr17:68511686-68512077 | Rare:107 | ||||
| chr17:68525588-68525912 | Common:1; Rare:61; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 |