| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:94683742-94683885 | Rare:45 | ||||
| chr10:94938492-94938838 | Rare:116 | ||||
| chr10:95069265-95069595 | Common:1; Rare:96 | ||||
| chr10:95290911-95291205 | Common:2; Rare:119 | ||||
| chr10:95561334-95561587 | Common:4; Rare:71 | ||||
| chr10:95693895-95694081 | Common:2; Rare:66; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr10:95907781-95907915 | Common:1; Rare:40 | ||||
| chr10:96043382-96043583 | Common:1; Rare:82 | ||||
| chr10:96129591-96129769 | Common:1; Rare:45 | ||||
| chr10:96129970-96130067 | Common:1; Rare:32 | ||||
| chr10:96130229-96130568 | Common:1; Rare:115 | ||||
| chr10:96586822-96586929 | Common:4; Rare:47 | ||||
| chr10:96720457-96720597 | Common:1; Rare:35 | ||||
| chr10:96831999-96832305 | Rare:118 | ||||
| chr10:97334699-97334830 | Common:1; Rare:54 |