| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:124801735-124801844 | Rare:36 | ||||
| chr10:125719453-125719769 | Common:1; Rare:116 | ||||
| chr10:125823179-125823594 | Common:2; Rare:150; Clinvar:1; Clinvar (benign):2 | ||||
| chr10:125881312-125881471 | Common:1; Rare:35 | ||||
| chr10:125896276-125896589 | Common:2; Rare:16 | ||||
| chr10:126670188-126670680 | Rare:124 | ||||
| chr10:126905271-126905465 | Rare:73 | ||||
| chr10:129466978-129467282 | Common:4; Rare:116; Clinvar:1 | ||||
| chr10:130136303-130136478 | Common:6; Rare:77 | ||||
| chr10:132331803-132332182 | Common:16; Rare:121 | ||||
| chr10:133308829-133308980 | Rare:71 | ||||
| chr10:133394000-133394325 | Common:2; Rare:141 | ||||
| chr11:207320-207726 | Common:8; Rare:136 | ||||
| chr11:208688-208855 | Rare:68 | ||||
| chr11:236326-236523 | Common:6; Rare:63 |