| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:124093532-124093733 | Common:2; Rare:39 | ||||
| chr10:124461720-124461865 | Common:4; Rare:53 | ||||
| chr10:124791756-124791941 | Common:1; Rare:97 | ||||
| chr10:124801751-124801841 | Rare:33 | ||||
| chr10:125719462-125719752 | Common:1; Rare:103 | ||||
| chr10:125823197-125823594 | Common:1; Rare:140; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:125896239-125896607 | Common:3; Rare:24 | ||||
| chr10:126905297-126905460 | Rare:63 | ||||
| chr10:130136327-130136487 | Common:7; Rare:65 | ||||
| chr10:132331761-132332193 | Common:18; Rare:140 | ||||
| chr10:133308835-133308991 | Rare:72 | ||||
| chr11:207338-207719 | Common:8; Rare:129 | ||||
| chr11:208662-208865 | Rare:79 | ||||
| chr11:236326-236525 | Common:6; Rare:64 | ||||
| chr11:236729-237059 | Common:4; Rare:107 |