| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:124801751-124801847 | Rare:36 | ||||
| chr10:125158771-125159002 | Rare:70 | ||||
| chr10:125719494-125719768 | Common:1; Rare:101 | ||||
| chr10:125823200-125823620 | Common:1; Rare:150; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:125896282-125896607 | Common:3; Rare:22 | ||||
| chr10:126905297-126905473 | Rare:69 | ||||
| chr10:132331847-132332213 | Common:12; Rare:105 | ||||
| chr10:133308829-133309094 | Common:2; Rare:107 | ||||
| chr10:133309148-133309432 | Common:2; Rare:109 | ||||
| chr10:133347063-133347422 | Rare:79 | ||||
| chr10:133393776-133394109 | Common:3; Rare:96 | ||||
| chr10:133565543-133565875 | Common:5; Rare:116 | ||||
| chr11:207332-207720 | Common:8; Rare:131 | ||||
| chr11:208662-208865 | Rare:79 | ||||
| chr11:236316-236522 | Common:6; Rare:69 |