| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4366601-4366837 | Common:1; Rare:97 | ||||
| chr17:4555326-4555525 | Common:3; Rare:92 | ||||
| chr17:4704116-4704311 | Rare:101 | ||||
| chr17:4731296-4731481 | Common:2; Rare:54 | ||||
| chr17:4806970-4807192 | Common:4; Rare:75 | ||||
| chr17:4899384-4899479 | Common:1; Rare:61; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:4939897-4940341 | Common:2; Rare:131 | ||||
| chr17:4947656-4947684 | Rare:13 | ||||
| chr17:4947910-4948015 | Rare:27 | ||||
| chr17:4948133-4948712 | Common:4; Rare:215 | ||||
| chr17:4948914-4949185 | Common:2; Rare:92 | ||||
| chr17:4950430-4950591 | Rare:36 | ||||
| chr17:4950806-4951211 | Common:2; Rare:89; Clinvar (benign):2 | ||||
| chr17:4951520-4951786 | Rare:54 | ||||
| chr17:4960521-4960839 | Common:1; Rare:72 |