| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:95290815-95291216 | Common:6; Rare:319 | ||||
| chr10:95561319-95561656 | Common:8; Rare:185 | ||||
| chr10:95656571-95657034 | Common:2; Rare:212; Clinvar:12; Clinvar (benign):8 | ||||
| chr10:95693625-95694078 | Common:4; Rare:216; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
| chr10:95907714-95908001 | Common:8; Rare:162 | ||||
| chr10:96043020-96043250 | Common:1; Rare:79 | ||||
| chr10:96043311-96043681 | Common:6; Rare:311 | ||||
| chr10:96129894-96130707 | Common:13; Rare:658 | ||||
| chr10:96130720-96131100 | Common:5; Rare:233 | ||||
| chr10:96271439-96271845 | Common:1; Rare:141 | ||||
| chr10:96513710-96514143 | Common:8; Rare:125 | ||||
| chr10:96586385-96586785 | Common:6; Rare:255 | ||||
| chr10:96586766-96587232 | Common:10; Rare:403 | ||||
| chr10:96587260-96587699 | Common:6; Rare:152 | ||||
| chr10:96633040-96633420 | Common:4; Rare:65 |