| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:63521102-63521576 | Common:8; Rare:158 | ||||
| chr10:67885143-67885374 | Common:1; Rare:82 | ||||
| chr10:68073934-68074223 | Common:1; Rare:51 | ||||
| chr10:68074730-68074999 | Common:2; Rare:62 | ||||
| chr10:68075155-68075466 | Common:4; Rare:125 | ||||
| chr10:68331986-68332233 | Common:1; Rare:88 | ||||
| chr10:68332876-68333409 | Common:2; Rare:111 | ||||
| chr10:68338501-68338927 | Common:1; Rare:95 | ||||
| chr10:68527407-68527580 | Common:2; Rare:58 | ||||
| chr10:68721136-68721534 | Common:4; Rare:121 | ||||
| chr10:68956061-68956309 | Common:2; Rare:83 | ||||
| chr10:68989002-68989117 | Common:1; Rare:32; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr10:69179914-69180301 | Common:2; Rare:120 | ||||
| chr10:69451350-69451527 | Common:2; Rare:42 | ||||
| chr10:69801624-69802004 | Common:2; Rare:96 |