| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:124418875-124419128 | Common:5; Rare:118; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:124791756-124791984 | Common:1; Rare:121 | ||||
| chr10:124801735-124801860 | Rare:44 | ||||
| chr10:125719446-125719764 | Common:1; Rare:114 | ||||
| chr10:125823200-125823573 | Common:1; Rare:125; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:126905290-126905465 | Rare:65 | ||||
| chr10:130136303-130136469 | Common:6; Rare:73 | ||||
| chr10:131981792-131982139 | Common:4; Rare:121 | ||||
| chr10:132331783-132332164 | Common:17; Rare:127 | ||||
| chr10:133308829-133308989 | Rare:75 | ||||
| chr10:133309156-133309417 | Common:2; Rare:99 | ||||
| chr10:133347076-133347422 | Rare:77 | ||||
| chr10:133526869-133527595 | Common:7; Rare:152 | ||||
| chr10:133528445-133528884 | Common:3; Rare:136 | ||||
| chr10:133531595-133531828 | Common:1; Rare:70 |