| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:63741774-63741906 | Common:2; Rare:44 | ||||
| chr17:63773466-63773858 | Common:2; Rare:127 | ||||
| chr17:63827057-63827522 | Common:5; Rare:135 | ||||
| chr17:64006739-64007059 | Rare:65 | ||||
| chr17:64020574-64020823 | Common:2; Rare:45 | ||||
| chr17:64390624-64391017 | Common:1; Rare:70 | ||||
| chr17:64506513-64506801 | Common:3; Rare:109 | ||||
| chr17:65056520-65056955 | Common:4; Rare:180 | ||||
| chr17:67044331-67044748 | Common:5; Rare:120 | ||||
| chr17:67245147-67245286 | Rare:45 | ||||
| chr17:67717744-67717970 | Rare:80 | ||||
| chr17:68247866-68248142 | Common:6; Rare:115 | ||||
| chr17:68291283-68291543 | Common:1; Rare:74 | ||||
| chr17:68511760-68512565 | Common:3; Rare:224; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:69327045-69327317 | Common:2; Rare:87 |