| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:124737633-124738033 | Common:1; Rare:86 | ||||
| chr11:124746856-124747256 | Rare:117 | ||||
| chr11:124799078-124799349 | Common:1; Rare:46 | ||||
| chr11:124920850-124921140 | Common:2; Rare:81; Clinvar:5; Clinvar (benign):2 | ||||
| chr11:124942573-124942703 | Common:1; Rare:28 | ||||
| chr11:124942760-124942970 | Rare:33 | ||||
| chr11:124943114-124943264 | Rare:29 | ||||
| chr11:125139775-125140220 | Common:2; Rare:118 | ||||
| chr11:125163481-125163864 | Common:1; Rare:75 | ||||
| chr11:125165815-125166467 | Common:6; Rare:198 | ||||
| chr11:125167368-125167642 | Common:2; Rare:58 | ||||
| chr11:125167943-125168194 | Common:2; Rare:44 | ||||
| chr11:125180315-125180715 | Common:3; Rare:88 | ||||
| chr11:125214630-125215270 | Common:6; Rare:131 | ||||
| chr11:125263280-125263730 | Common:4; Rare:107 |