| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:12043134-12043323 | Common:2; Rare:46 | ||||
| chr10:12068697-12069058 | Common:2; Rare:134 | ||||
| chr10:12195767-12195987 | Rare:55 | ||||
| chr10:12349500-12349812 | Common:2; Rare:91 | ||||
| chr10:13099929-13100298 | Common:4; Rare:85; Clinvar:3; Clinvar (benign):6 | ||||
| chr10:13300009-13300120 | Rare:44; Clinvar:2 | ||||
| chr10:13348005-13348409 | Rare:132 | ||||
| chr10:13348540-13348594 | Rare:15 | ||||
| chr10:14837987-14838408 | Common:4; Rare:123 | ||||
| chr10:14838854-14838957 | Rare:23 | ||||
| chr10:14878597-14878922 | Common:2; Rare:105 | ||||
| chr10:14954023-14954205 | Rare:66 | ||||
| chr10:15088727-15088930 | Common:1; Rare:85 | ||||
| chr10:15097307-15097436 | Common:1; Rare:52 | ||||
| chr10:15860308-15860611 | Common:1; Rare:77 |