| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33774493-33774670 | Common:2; Rare:62 | ||||
| chr11:34051619-34051789 | Rare:74 | ||||
| chr11:34052207-34052610 | Common:4; Rare:191 | ||||
| chr11:34438784-34438972 | Common:1; Rare:58 | ||||
| chr11:34916287-34916661 | Common:10; Rare:151; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35138949-35139207 | Common:1; Rare:57 | ||||
| chr11:35525567-35525766 | Rare:57 | ||||
| chr11:35663184-35663500 | Rare:122 | ||||
| chr11:36455738-36456077 | Rare:69 | ||||
| chr11:36510236-36510386 | Rare:45 | ||||
| chr11:43358831-43359059 | Rare:102 | ||||
| chr11:43680316-43680622 | Common:6; Rare:77 | ||||
| chr11:43880674-43880889 | Common:2; Rare:53 | ||||
| chr11:46277882-46278213 | Rare:87 | ||||
| chr11:46377816-46378021 | Common:1; Rare:29 |