| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:97498346-97498550 | Common:2; Rare:93 | ||||
| chr10:97498696-97499075 | Common:2; Rare:110 | ||||
| chr10:97687378-97687631 | Common:2; Rare:75 | ||||
| chr10:97713428-97713829 | Rare:101 | ||||
| chr10:97714283-97714445 | Rare:52 | ||||
| chr10:97849776-97849993 | Common:1; Rare:62 | ||||
| chr10:98425548-98425835 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr10:98446132-98446381 | Common:1; Rare:51 | ||||
| chr10:98446761-98447008 | Rare:67; Clinvar:1 | ||||
| chr10:99430556-99430941 | Common:4; Rare:94 | ||||
| chr10:99659185-99659579 | Common:2; Rare:103 | ||||
| chr10:99732005-99732369 | Rare:137; Clinvar:5; Clinvar (benign):1 | ||||
| chr10:100185920-100186102 | Rare:73 | ||||
| chr10:100229516-100229660 | Rare:53 | ||||
| chr10:100286600-100286934 | Common:5; Rare:128 |