| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44829930-44830060 | Rare:32 | ||||
| chr17:44830135-44830454 | Common:1; Rare:125 | ||||
| chr17:44899383-44899741 | Common:2; Rare:112; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:45060992-45061353 | Common:2; Rare:102 | ||||
| chr17:45132340-45132638 | Common:2; Rare:89 | ||||
| chr17:45148152-45148637 | Common:1; Rare:165 | ||||
| chr17:45161543-45161918 | Common:1; Rare:93 | ||||
| chr17:45620248-45620367 | Rare:31 | ||||
| chr17:46193330-46193604 | Common:5; Rare:78 | ||||
| chr17:46922869-46923187 | Common:3; Rare:89; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47188849-47189036 | Common:1; Rare:38 | ||||
| chr17:47189246-47189538 | Rare:75 | ||||
| chr17:47253696-47253931 | Common:4; Rare:72; Clinvar:1; Clinvar (benign):4 | ||||
| chr17:47323861-47324034 | Common:2; Rare:65 | ||||
| chr17:47649518-47649965 | Common:1; Rare:163 |