| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:352768-352858 | Common:1; Rare:19 | ||||
| chr17:714687-714966 | Common:4; Rare:95; Clinvar (benign):1 | ||||
| chr17:732311-732641 | Common:2; Rare:118 | ||||
| chr17:1011935-1012061 | Common:1; Rare:62 | ||||
| chr17:1012727-1013027 | Common:2; Rare:105 | ||||
| chr17:1031803-1032104 | Common:4; Rare:71 | ||||
| chr17:1456113-1456456 | Common:4; Rare:134 | ||||
| chr17:1467894-1468127 | Common:2; Rare:101; Clinvar (benign):5 | ||||
| chr17:1480533-1480729 | Common:1; Rare:65; Clinvar (benign):2 | ||||
| chr17:1516550-1516949 | Common:2; Rare:139 | ||||
| chr17:1628373-1628652 | Rare:89 | ||||
| chr17:1628793-1628991 | Rare:69 | ||||
| chr17:1716158-1716544 | Common:3; Rare:123 | ||||
| chr17:1829780-1830042 | Common:8; Rare:112 | ||||
| chr17:2303319-2303390 | Rare:25 |