| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:18651576-18651683 | Common:1; Rare:38 | ||||
| chr10:27154323-27154469 | Rare:41 | ||||
| chr10:27155227-27155436 | Common:6; Rare:94; Clinvar:2; Clinvar (benign):6 | ||||
| chr10:27240740-27240889 | Rare:40 | ||||
| chr10:31031848-31032052 | Common:2; Rare:83 | ||||
| chr10:31319012-31319244 | Common:2; Rare:70 | ||||
| chr10:31928742-31928913 | Common:3; Rare:68 | ||||
| chr10:32056364-32056555 | Common:1; Rare:79 | ||||
| chr10:32378724-32378854 | Rare:20 | ||||
| chr10:32446044-32446166 | Common:1; Rare:55 | ||||
| chr10:32958149-32958524 | Common:2; Rare:140 | ||||
| chr10:35126639-35127163 | Common:4; Rare:171 | ||||
| chr10:38010636-38010746 | Common:1; Rare:52 | ||||
| chr10:42638520-42638624 | Common:2; Rare:47 | ||||
| chr10:42782669-42782817 | Rare:39 |