| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:93893842-93894058 | Common:1; Rare:84 | ||||
| chr10:93993740-93993967 | Common:2; Rare:60 | ||||
| chr10:93994076-93994208 | Common:1; Rare:31; Clinvar:3; Clinvar (benign):1 | ||||
| chr10:93994293-93994416 | Rare:30 | ||||
| chr10:94362445-94362560 | Common:1; Rare:26 | ||||
| chr10:94362806-94363156 | Common:6; Rare:133 | ||||
| chr10:94402097-94402625 | Rare:145 | ||||
| chr10:94402737-94402963 | Common:2; Rare:84 | ||||
| chr10:94545145-94545472 | Rare:59 | ||||
| chr10:94545593-94545939 | Common:4; Rare:107 | ||||
| chr10:94546405-94546456 | Rare:17 | ||||
| chr10:95273695-95273845 | Rare:28 | ||||
| chr10:95290464-95290643 | Common:1; Rare:31 | ||||
| chr10:95290844-95291331 | Common:4; Rare:174 | ||||
| chr10:95560840-95560956 | Rare:22 |