| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:125823200-125823585 | Common:1; Rare:132; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:126905290-126905479 | Rare:73 | ||||
| chr10:131981874-131982154 | Common:3; Rare:106 | ||||
| chr10:132331810-132332155 | Common:14; Rare:110 | ||||
| chr10:133308835-133308980 | Rare:68 | ||||
| chr10:133394030-133394290 | Common:2; Rare:116 | ||||
| chr11:207352-207720 | Common:8; Rare:125 | ||||
| chr11:208688-208865 | Rare:72 | ||||
| chr11:320729-320900 | Common:5; Rare:65; Clinvar:1 | ||||
| chr11:777463-777598 | Common:1; Rare:59 | ||||
| chr11:842497-842895 | Common:7; Rare:163 | ||||
| chr11:2902065-2902308 | Common:1; Rare:54 | ||||
| chr11:2929417-2929540 | Rare:20 | ||||
| chr11:2992228-2992528 | Common:2; Rare:115 | ||||
| chr11:3057363-3057545 | Rare:65 |