| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:124461714-124461873 | Common:4; Rare:58 | ||||
| chr10:124791745-124791959 | Common:1; Rare:112 | ||||
| chr10:125003712-125003915 | Common:4; Rare:45 | ||||
| chr10:125719446-125719820 | Common:1; Rare:139 | ||||
| chr10:125823103-125823626 | Common:2; Rare:187; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:125896239-125896628 | Common:5; Rare:31 | ||||
| chr10:126905297-126905562 | Rare:99 | ||||
| chr10:129466974-129467324 | Common:4; Rare:131; Clinvar:1 | ||||
| chr10:130136321-130136495 | Common:7; Rare:68 | ||||
| chr10:131981865-131982200 | Common:5; Rare:128 | ||||
| chr10:132331816-132332269 | Common:13; Rare:150 | ||||
| chr10:132785553-132785763 | Rare:52; Clinvar (pathogenic):1 | ||||
| chr10:132942535-132942693 | Common:2; Rare:49 | ||||
| chr10:133276837-133277022 | Rare:47 | ||||
| chr10:133308835-133308989 | Rare:72 |