| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:5486802-5486916 | Common:4; Rare:33 | ||||
| chr17:6640651-6641097 | Common:7; Rare:140 | ||||
| chr17:6651557-6651747 | Common:1; Rare:65 | ||||
| chr17:6755902-6756074 | Common:3; Rare:43 | ||||
| chr17:7012297-7012685 | Rare:133 | ||||
| chr17:7234472-7234688 | Common:2; Rare:111 | ||||
| chr17:7242272-7242584 | Common:1; Rare:103 | ||||
| chr17:7251967-7252313 | Common:1; Rare:133 | ||||
| chr17:7262390-7262649 | Rare:56 | ||||
| chr17:7438166-7438298 | Common:1; Rare:28 | ||||
| chr17:7484239-7484370 | Common:1; Rare:53 | ||||
| chr17:7558697-7559035 | Common:1; Rare:69 | ||||
| chr17:7583530-7583865 | Common:1; Rare:135; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7627799-7627996 | Common:2; Rare:63 | ||||
| chr17:7717618-7717760 | Rare:35 |