| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:122954197-122954479 | Rare:104 | ||||
| chr10:123008799-123009032 | Common:5; Rare:68; Clinvar:4; Clinvar (benign):5 | ||||
| chr10:125719462-125719734 | Common:1; Rare:86 | ||||
| chr10:125823211-125823566 | Common:1; Rare:116; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:126905297-126905458 | Rare:62 | ||||
| chr10:133308829-133308989 | Rare:75 | ||||
| chr11:207361-207726 | Common:7; Rare:112 | ||||
| chr11:208662-208873 | Rare:83 | ||||
| chr11:236333-236491 | Common:6; Rare:45 | ||||
| chr11:236755-237040 | Common:4; Rare:95 | ||||
| chr11:506751-506981 | Common:2; Rare:76 | ||||
| chr11:576412-576531 | Rare:48 | ||||
| chr11:695639-695818 | Rare:45 | ||||
| chr11:764063-764339 | Common:1; Rare:67 | ||||
| chr11:777458-777607 | Common:1; Rare:65 |