| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:91909380-91909614 | Common:1; Rare:43 | ||||
| chr10:91923693-91923877 | Common:1; Rare:82 | ||||
| chr10:92291014-92291497 | Common:6; Rare:156 | ||||
| chr10:92573951-92574132 | Common:1; Rare:63 | ||||
| chr10:92592952-92593178 | Common:3; Rare:66 | ||||
| chr10:92689744-92689963 | Common:1; Rare:73 | ||||
| chr10:92848303-92848531 | Rare:85 | ||||
| chr10:93073473-93073960 | Common:2; Rare:118 | ||||
| chr10:93496369-93496705 | Common:5; Rare:88 | ||||
| chr10:93702298-93702619 | Common:5; Rare:97 | ||||
| chr10:94545668-94545949 | Common:4; Rare:97 | ||||
| chr10:95290837-95291178 | Common:2; Rare:133 | ||||
| chr10:95656599-95656930 | Common:1; Rare:89; Clinvar:6; Clinvar (benign):2 | ||||
| chr10:95693802-95694067 | Common:2; Rare:101; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr10:95907684-95907947 | Common:3; Rare:73 |