| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:56833484-56833722 | Common:3; Rare:76 | ||||
| chr17:56833724-56834268 | Common:6; Rare:172 | ||||
| chr17:56834465-56834507 | Common:2; Rare:9 | ||||
| chr17:56834534-56834578 | Common:1; Rare:9 | ||||
| chr17:56834608-56834789 | Rare:49 | ||||
| chr17:56834809-56835057 | Common:2; Rare:103; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr17:56912636-56912706 | Rare:12 | ||||
| chr17:56913388-56913411 | Rare:9 | ||||
| chr17:56913640-56913760 | Common:1; Rare:43 | ||||
| chr17:56913772-56914621 | Common:4; Rare:205 | ||||
| chr17:56960520-56960702 | Common:5; Rare:35 | ||||
| chr17:56960742-56960849 | Rare:50 | ||||
| chr17:56960948-56961181 | Common:3; Rare:78 | ||||
| chr17:56977741-56977799 | Rare:13 | ||||
| chr17:56978011-56978242 | Common:3; Rare:107 |