| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:95290819-95291170 | Common:2; Rare:133 | ||||
| chr10:95693856-95694153 | Common:5; Rare:104; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr10:95907766-95907923 | Common:1; Rare:43 | ||||
| chr10:95908113-95908205 | Rare:18 | ||||
| chr10:96129962-96130067 | Common:1; Rare:36 | ||||
| chr10:96130163-96130657 | Common:2; Rare:159 | ||||
| chr10:96271394-96271615 | Common:1; Rare:55 | ||||
| chr10:96586529-96586764 | Common:1; Rare:66 | ||||
| chr10:96832060-96832308 | Rare:98 | ||||
| chr10:97334683-97334843 | Common:2; Rare:69 | ||||
| chr10:97426044-97426308 | Common:2; Rare:121 | ||||
| chr10:97427670-97427761 | Rare:19 | ||||
| chr10:97445933-97446229 | Common:1; Rare:85 | ||||
| chr10:97498356-97498550 | Common:2; Rare:85 | ||||
| chr10:97498694-97498947 | Common:2; Rare:73 |