| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:50991102-50991381 | Common:4; Rare:79 | ||||
| chr10:51074019-51074328 | Common:5; Rare:76 | ||||
| chr10:51074371-51074763 | Common:1; Rare:95; Clinvar (benign):10 | ||||
| chr10:51699557-51699920 | Common:6; Rare:93 | ||||
| chr10:56361217-56361459 | Common:6; Rare:78 | ||||
| chr10:58267898-58268066 | Rare:51 | ||||
| chr10:58268972-58269274 | Common:4; Rare:96 | ||||
| chr10:58385316-58385499 | Common:2; Rare:65 | ||||
| chr10:59176447-59176654 | Common:4; Rare:69 | ||||
| chr10:59362487-59362698 | Common:1; Rare:58 | ||||
| chr10:59906389-59906642 | Common:2; Rare:69 | ||||
| chr10:60300531-60300799 | Common:1; Rare:46 | ||||
| chr10:60733428-60733535 | Rare:31 | ||||
| chr10:60778332-60778510 | Common:1; Rare:39 | ||||
| chr10:61662873-61662942 | Rare:15 |