| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:86756215-86756817 | Common:4; Rare:188; Clinvar:1 | ||||
| chr10:86756916-86757032 | Rare:32; Clinvar (benign):2 | ||||
| chr10:87094023-87094197 | Rare:47 | ||||
| chr10:87094737-87095340 | Common:2; Rare:163; Clinvar:3 | ||||
| chr10:87095341-87095650 | Common:2; Rare:75 | ||||
| chr10:87095669-87095809 | Rare:35 | ||||
| chr10:87504622-87504932 | Common:4; Rare:109 | ||||
| chr10:87660032-87660188 | Common:2; Rare:43 | ||||
| chr10:87817465-87817730 | Rare:54 | ||||
| chr10:87817736-87818008 | Rare:67 | ||||
| chr10:87818091-87818537 | Common:3; Rare:124 | ||||
| chr10:87862206-87862855 | Rare:257; Clinvar:1 | ||||
| chr10:87863062-87863377 | Rare:90; Clinvar:39; Clinvar (benign):2 | ||||
| chr10:87863463-87863724 | Common:1; Rare:85; Clinvar:54; Clinvar (benign):4 | ||||
| chr10:87863871-87863886 | Rare:4 |