| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15251201-15251544 | Common:2; Rare:56 | ||||
| chr17:15261584-15261616 | Rare:4 | ||||
| chr17:16056365-16056489 | Common:2; Rare:25 | ||||
| chr17:16061860-16062046 | Common:1; Rare:49 | ||||
| chr17:17495630-17495786 | Rare:49 | ||||
| chr17:17836286-17836433 | Common:2; Rare:33 | ||||
| chr17:29677160-29677447 | Common:1; Rare:32 | ||||
| chr17:31008496-31008605 | Common:1; Rare:22 | ||||
| chr17:39727529-39727849 | Common:1; Rare:99; Clinvar:4 | ||||
| chr17:40096074-40096135 | Rare:23 | ||||
| chr17:40099215-40099457 | Common:2; Rare:68 | ||||
| chr17:42222093-42222120 | Rare:6 | ||||
| chr17:42422614-42422804 | Rare:81; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr17:42422813-42422974 | Rare:61; Clinvar:2 | ||||
| chr17:43315656-43315916 | Common:6; Rare:110 |