| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:68407179-68407442 | Common:5; Rare:89 | ||||
| chr10:68527432-68527574 | Common:2; Rare:49 | ||||
| chr10:68720934-68721288 | Common:2; Rare:113 | ||||
| chr10:68721472-68721739 | Common:1; Rare:83 | ||||
| chr10:68900988-68901374 | Common:3; Rare:153 | ||||
| chr10:68956093-68956436 | Common:3; Rare:110 | ||||
| chr10:68988630-68989105 | Common:4; Rare:137; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr10:69179907-69180341 | Common:3; Rare:144 | ||||
| chr10:69318558-69318945 | Common:5; Rare:107 | ||||
| chr10:69630125-69630312 | Common:1; Rare:59 | ||||
| chr10:70052700-70052996 | Rare:66 | ||||
| chr10:70146616-70146978 | Common:2; Rare:90 | ||||
| chr10:70170428-70170713 | Common:4; Rare:92 | ||||
| chr10:70382585-70382778 | Common:5; Rare:73 | ||||
| chr10:71319177-71319299 | Common:2; Rare:46; Clinvar:2; Clinvar (benign):1 |