| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:12349329-12349534 | Common:1; Rare:52 | ||||
| chr10:12349536-12349727 | Common:1; Rare:52 | ||||
| chr10:12349742-12349932 | Common:1; Rare:57 | ||||
| chr10:13001699-13001882 | Rare:55 | ||||
| chr10:13099317-13099593 | Common:1; Rare:53 | ||||
| chr10:13099770-13099817 | Rare:13 | ||||
| chr10:13099930-13100176 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):3 | ||||
| chr10:13161258-13161649 | Common:1; Rare:107 | ||||
| chr10:13161799-13161953 | Common:2; Rare:27 | ||||
| chr10:13299982-13300215 | Rare:81; Clinvar:2 | ||||
| chr10:13302060-13302222 | Common:2; Rare:23 | ||||
| chr10:13302276-13302597 | Rare:66 | ||||
| chr10:13346806-13347085 | Common:6; Rare:68 | ||||
| chr10:13347267-13347534 | Common:2; Rare:94 | ||||
| chr10:13347654-13347883 | Common:2; Rare:67 |