| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:125719453-125719757 | Common:1; Rare:107 | ||||
| chr10:125823200-125823620 | Common:1; Rare:150; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:125896462-125896615 | Common:3; Rare:13 | ||||
| chr10:126905268-126905473 | Rare:81 | ||||
| chr10:127987179-127987281 | Rare:20 | ||||
| chr10:130136325-130136457 | Common:6; Rare:55 | ||||
| chr10:131981910-131982154 | Common:1; Rare:90 | ||||
| chr10:132331847-132332213 | Common:12; Rare:105 | ||||
| chr10:133308835-133308989 | Rare:72 | ||||
| chr10:133565533-133565719 | Common:3; Rare:74 | ||||
| chr11:207352-207740 | Common:9; Rare:133 | ||||
| chr11:208763-208876 | Rare:47 | ||||
| chr11:236324-236559 | Common:8; Rare:81 | ||||
| chr11:236834-237039 | Common:2; Rare:74 | ||||
| chr11:288817-289169 | Common:3; Rare:97 |