| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45620130-45620580 | Common:2; Rare:194 | ||||
| chr17:45894196-45894685 | Common:20; Rare:657; Clinvar:23; Clinvar (benign):11 | ||||
| chr17:46191962-46193275 | Common:43; Rare:730; Clinvar (benign):28 | ||||
| chr17:46193290-46193760 | Common:41; Rare:681 | ||||
| chr17:46193905-46194310 | Common:20; Rare:195 | ||||
| chr17:46225231-46225651 | Common:18; Rare:298 | ||||
| chr17:46818551-46818951 | Rare:164; Clinvar:5 | ||||
| chr17:46819101-46819932 | Common:1; Rare:238 | ||||
| chr17:46832892-46833292 | Common:6; Rare:154 | ||||
| chr17:46922641-46923231 | Common:18; Rare:560; Clinvar:7; Clinvar (benign):38; Clinvar (pathogenic):1 | ||||
| chr17:47188283-47188818 | Common:2; Rare:168 | ||||
| chr17:47188755-47188882 | Common:2; Rare:22 | ||||
| chr17:47188880-47189090 | Common:4; Rare:73 | ||||
| chr17:47189077-47189745 | Common:4; Rare:798 | ||||
| chr17:47199996-47200396 | Common:1; Rare:55 |