| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100267601-100267682 | Common:2; Rare:36 | ||||
| chr10:100286533-100286725 | Common:4; Rare:98 | ||||
| chr10:100347065-100347482 | Common:3; Rare:105 | ||||
| chr10:100529637-100530010 | Common:2; Rare:108 | ||||
| chr10:100912730-100913011 | Common:1; Rare:89 | ||||
| chr10:100913328-100913436 | Rare:30 | ||||
| chr10:100987222-100987613 | Common:2; Rare:141; Clinvar:1; Clinvar (benign):2 | ||||
| chr10:101031093-101031483 | Common:1; Rare:89 | ||||
| chr10:101588166-101588339 | Rare:72 | ||||
| chr10:101818353-101818770 | Common:1; Rare:110 | ||||
| chr10:101839803-101840094 | Common:1; Rare:84 | ||||
| chr10:102056100-102056368 | Common:1; Rare:64 | ||||
| chr10:102114936-102115128 | Common:2; Rare:55 | ||||
| chr10:102152100-102152423 | Common:3; Rare:107 | ||||
| chr10:102245216-102245590 | Common:1; Rare:70 |