| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:94362881-94363129 | Common:5; Rare:98 | ||||
| chr10:94402279-94402620 | Rare:110 | ||||
| chr10:94545145-94545365 | Rare:39 | ||||
| chr10:94545377-94545524 | Rare:29 | ||||
| chr10:94545592-94545895 | Common:4; Rare:89 | ||||
| chr10:95290493-95290774 | Common:1; Rare:60 | ||||
| chr10:95290922-95291286 | Common:3; Rare:137 | ||||
| chr10:95291399-95291459 | Rare:7 | ||||
| chr10:95561342-95561623 | Common:4; Rare:87 | ||||
| chr10:95656592-95657008 | Common:1; Rare:112; Clinvar:6; Clinvar (benign):3 | ||||
| chr10:95693814-95694079 | Common:2; Rare:99; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr10:95755512-95755758 | Common:1; Rare:46 | ||||
| chr10:95756033-95756193 | Common:1; Rare:36 | ||||
| chr10:95756504-95756623 | Common:1; Rare:29 | ||||
| chr10:95907822-95907991 | Common:3; Rare:51 |