| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:80036201-80036850 | Common:10; Rare:306; Clinvar:2; Clinvar (benign):6 | ||||
| chr17:80101391-80101685 | Common:10; Rare:245; Clinvar (benign):10 | ||||
| chr17:80147139-80147422 | Common:12; Rare:207 | ||||
| chr17:80178308-80178605 | Common:9; Rare:104 | ||||
| chr17:80187330-80187900 | Common:2; Rare:170 | ||||
| chr17:80219500-80219707 | Rare:37 | ||||
| chr17:80220279-80220471 | Common:1; Rare:134; Clinvar:2; Clinvar (pathogenic):4 | ||||
| chr17:80260436-80260979 | Common:24; Rare:124 | ||||
| chr17:80415032-80415201 | Common:2; Rare:107 | ||||
| chr17:80415107-80415209 | Common:1; Rare:74 | ||||
| chr17:80415375-80415518 | Common:8; Rare:94 | ||||
| chr17:80476562-80476765 | Rare:91 | ||||
| chr17:80544771-80545143 | Common:2; Rare:112 | ||||
| chr17:80545200-80545640 | Common:10; Rare:172 | ||||
| chr17:80991797-80991925 | Common:1; Rare:49 |