| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:124801730-124801843 | Rare:38 | ||||
| chr10:125719423-125719780 | Common:1; Rare:138 | ||||
| chr10:125823179-125823722 | Common:2; Rare:194; Clinvar:1; Clinvar (benign):2 | ||||
| chr10:125896284-125896599 | Common:2; Rare:18 | ||||
| chr10:126905271-126905474 | Rare:78 | ||||
| chr10:128047439-128047640 | Common:4; Rare:66 | ||||
| chr10:129466974-129467285 | Common:4; Rare:120; Clinvar:1 | ||||
| chr10:132331723-132332275 | Common:18; Rare:191 | ||||
| chr10:132916657-132916766 | Common:1; Rare:32 | ||||
| chr10:133308829-133309033 | Common:1; Rare:93 | ||||
| chr10:133393993-133394316 | Common:2; Rare:141 | ||||
| chr11:207332-207740 | Common:9; Rare:139 | ||||
| chr11:208476-208852 | Common:1; Rare:112 | ||||
| chr11:236324-236559 | Common:8; Rare:81 | ||||
| chr11:236913-237052 | Common:1; Rare:54 |