| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:125823194-125823625 | Common:1; Rare:154; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:125896391-125896583 | Common:2; Rare:7 | ||||
| chr10:126905286-126905487 | Rare:78 | ||||
| chr10:127906888-127907082 | Common:1; Rare:57 | ||||
| chr10:128047407-128047635 | Common:2; Rare:74 | ||||
| chr10:128126321-128126667 | Common:2; Rare:102 | ||||
| chr10:129466972-129467343 | Common:4; Rare:137; Clinvar:1 | ||||
| chr10:129964262-129964419 | Rare:43 | ||||
| chr10:130136260-130136464 | Common:7; Rare:87 | ||||
| chr10:131900477-131900694 | Common:2; Rare:63 | ||||
| chr10:131900852-131901013 | Rare:54 | ||||
| chr10:131981918-131982219 | Common:3; Rare:118 | ||||
| chr10:132186720-132186960 | Common:10; Rare:65 | ||||
| chr10:132249041-132249182 | Common:4; Rare:101 | ||||
| chr10:132307938-132308191 | Common:5; Rare:69 |