| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:17787734-17787929 | Common:3; Rare:32 | ||||
| chr10:18145023-18145164 | Common:1; Rare:26 | ||||
| chr10:18158011-18158273 | Common:1; Rare:40 | ||||
| chr10:18158805-18158958 | Common:1; Rare:33 | ||||
| chr10:18527634-18527889 | Common:2; Rare:68; Clinvar:3; Clinvar (benign):3 | ||||
| chr10:18627467-18627553 | Common:1; Rare:28 | ||||
| chr10:18627563-18627632 | Rare:26 | ||||
| chr10:18627761-18627789 | Rare:13 | ||||
| chr10:18627793-18627934 | Common:1; Rare:41 | ||||
| chr10:18650601-18650815 | Common:1; Rare:48 | ||||
| chr10:18658410-18658457 | Common:1; Rare:8 | ||||
| chr10:18659969-18660124 | Common:2; Rare:45 | ||||
| chr10:18660300-18660439 | Rare:39 | ||||
| chr10:18666945-18667076 | Common:1; Rare:28 | ||||
| chr10:18682040-18682080 | Rare:9 |