| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:69467393-69467602 | Common:1; Rare:40 | ||||
| chr17:69539897-69539921 | |||||
| chr17:69607152-69607458 | Rare:53 | ||||
| chr17:71362178-71362286 | Rare:22 | ||||
| chr17:72008545-72008890 | Common:2; Rare:52 | ||||
| chr17:72030149-72030397 | Common:1; Rare:46 | ||||
| chr17:72030438-72030838 | Common:3; Rare:82 | ||||
| chr17:72030859-72030957 | Common:3; Rare:26 | ||||
| chr17:72031263-72031334 | Rare:14 | ||||
| chr17:72122189-72122220 | Rare:8 | ||||
| chr17:72122658-72122844 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
| chr17:72297451-72297616 | Rare:33 | ||||
| chr17:72339018-72339326 | Common:1; Rare:55 | ||||
| chr17:72342587-72342962 | Common:2; Rare:70 | ||||
| chr17:72377027-72377072 | Rare:10 |