| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75457360-75457569 | Rare:38 | ||||
| chr17:75581176-75581349 | Rare:41 | ||||
| chr17:75589122-75589695 | Common:18; Rare:167 | ||||
| chr17:75753703-75753943 | Common:1; Rare:69; Clinvar:1 | ||||
| chr17:75775465-75775764 | Common:1; Rare:67 | ||||
| chr17:75827579-75827844 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:75827956-75828054 | Common:2; Rare:43; Clinvar:7; Clinvar (benign):3 | ||||
| chr17:75828235-75828308 | Rare:20 | ||||
| chr17:75895863-75895934 | Rare:13 | ||||
| chr17:75979927-75980047 | Common:1; Rare:23 | ||||
| chr17:75983568-75983854 | Rare:53 | ||||
| chr17:76143432-76143526 | Rare:14 | ||||
| chr17:76268313-76268459 | Rare:41 | ||||
| chr17:76345596-76345747 | Common:1; Rare:25 | ||||
| chr17:76444904-76445106 | Common:1; Rare:33 |