| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100996946-100997138 | Common:1; Rare:51 | ||||
| chr10:100998107-100998596 | Common:4; Rare:106 | ||||
| chr10:100999674-100999936 | Common:1; Rare:76 | ||||
| chr10:101031102-101031308 | Common:1; Rare:45 | ||||
| chr10:101031396-101031533 | Rare:34 | ||||
| chr10:101036500-101036806 | Rare:81 | ||||
| chr10:101037035-101037458 | Common:1; Rare:129 | ||||
| chr10:101061867-101062019 | Rare:29 | ||||
| chr10:101588140-101588339 | Rare:81 | ||||
| chr10:101694865-101695244 | Common:1; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:101817921-101818224 | Common:1; Rare:104 | ||||
| chr10:101818234-101818787 | Common:1; Rare:148 | ||||
| chr10:102056089-102056375 | Common:1; Rare:70 | ||||
| chr10:102110635-102110893 | Rare:72 | ||||
| chr10:102114925-102115039 | Common:1; Rare:43 |