| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75289387-75289638 | Common:2; Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:75393820-75394023 | Common:1; Rare:52 | ||||
| chr17:75515474-75515667 | Common:3; Rare:53 | ||||
| chr17:75516402-75516563 | Rare:47; Clinvar (pathogenic):1 | ||||
| chr17:75525483-75525811 | Common:3; Rare:105 | ||||
| chr17:75559023-75559397 | Rare:102 | ||||
| chr17:75568627-75568796 | Rare:71 | ||||
| chr17:75588185-75588488 | Common:2; Rare:83 | ||||
| chr17:75610474-75610959 | Common:3; Rare:96 | ||||
| chr17:75612789-75613044 | Common:3; Rare:75 | ||||
| chr17:75613600-75613858 | Common:3; Rare:81 | ||||
| chr17:75614584-75614847 | Rare:96 | ||||
| chr17:75615164-75615347 | Rare:48 | ||||
| chr17:75615780-75616193 | Common:3; Rare:98 | ||||
| chr17:75617144-75617539 | Common:1; Rare:99 |