| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:110497351-110497568 | Rare:56 | ||||
| chr10:110497601-110498034 | Common:5; Rare:137 | ||||
| chr10:110498113-110498164 | Rare:18 | ||||
| chr10:110498193-110498418 | Common:1; Rare:95 | ||||
| chr10:110567250-110567823 | Common:4; Rare:192; Clinvar:2; Clinvar (benign):5 | ||||
| chr10:110567905-110567966 | Common:2; Rare:12 | ||||
| chr10:110568052-110568127 | Rare:20 | ||||
| chr10:110568195-110568585 | Common:5; Rare:96 | ||||
| chr10:110871568-110872131 | Rare:182 | ||||
| chr10:110872178-110872395 | Rare:64 | ||||
| chr10:110918410-110918834 | Common:4; Rare:118 | ||||
| chr10:110918850-110919410 | Common:4; Rare:149 | ||||
| chr10:110919539-110919917 | Common:3; Rare:119; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:110920187-110920384 | Common:1; Rare:44 | ||||
| chr10:112183673-112183957 | Common:3; Rare:97 |