| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:124418892-124419092 | Common:4; Rare:91; Clinvar:3; Clinvar (benign):1 | ||||
| chr10:124791750-124791941 | Common:1; Rare:99 | ||||
| chr10:125719442-125719744 | Common:1; Rare:104 | ||||
| chr10:125823192-125823567 | Common:1; Rare:124; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:125896472-125896628 | Common:3; Rare:17 | ||||
| chr10:126388134-126388257 | Rare:32 | ||||
| chr10:126905290-126905479 | Rare:73 | ||||
| chr10:132331795-132332178 | Common:16; Rare:123 | ||||
| chr10:133308829-133308974 | Rare:69 | ||||
| chr11:207292-207768 | Common:9; Rare:155 | ||||
| chr11:208598-208852 | Common:1; Rare:89 | ||||
| chr11:236326-236559 | Common:8; Rare:79 | ||||
| chr11:236689-237049 | Common:4; Rare:113 | ||||
| chr11:307579-307792 | Common:6; Rare:61 | ||||
| chr11:320558-320936 | Common:5; Rare:147; Clinvar:1 |