| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7584018-7584166 | Rare:89 | ||||
| chr17:7614789-7614969 | Rare:107 | ||||
| chr17:7627759-7628019 | Common:8; Rare:204 | ||||
| chr17:7685990-7686716 | Common:1; Rare:362 | ||||
| chr17:7687115-7687380 | Common:1; Rare:84; Clinvar (benign):1 | ||||
| chr17:7687413-7687658 | Rare:138; Clinvar:6 | ||||
| chr17:7688101-7688578 | Common:6; Rare:173; Clinvar:7; Clinvar (benign):4 | ||||
| chr17:7705000-7705230 | Common:2; Rare:50 | ||||
| chr17:7716444-7717370 | Common:5; Rare:207 | ||||
| chr17:7717286-7717433 | Common:1; Rare:26 | ||||
| chr17:7717556-7717674 | Common:4; Rare:53 | ||||
| chr17:7740430-7740863 | Common:1; Rare:288 | ||||
| chr17:7804085-7804285 | Rare:59 | ||||
| chr17:7843640-7843805 | Rare:99 | ||||
| chr17:7843836-7844210 | Common:11; Rare:262 |