| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:125823180-125823577 | Common:2; Rare:138; Clinvar:1; Clinvar (benign):2 | ||||
| chr10:126905153-126905481 | Common:2; Rare:120 | ||||
| chr10:131981886-131982127 | Common:2; Rare:87 | ||||
| chr10:132331818-132332116 | Common:11; Rare:94 | ||||
| chr10:133308829-133308960 | Rare:62 | ||||
| chr11:207343-207746 | Common:9; Rare:138 | ||||
| chr11:208620-208854 | Rare:84 | ||||
| chr11:236315-236546 | Common:8; Rare:81 | ||||
| chr11:236689-237022 | Common:3; Rare:98 | ||||
| chr11:320667-320937 | Common:5; Rare:108; Clinvar:1 | ||||
| chr11:506676-507001 | Common:3; Rare:102 | ||||
| chr11:575819-576173 | Common:4; Rare:79 | ||||
| chr11:576431-576500 | Rare:22 | ||||
| chr11:695503-695826 | Common:1; Rare:92 | ||||
| chr11:706517-706647 | Rare:22 |