| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:127001145-127001367 | Common:4; Rare:59 | ||||
| chr11:127003343-127003695 | Common:1; Rare:83 | ||||
| chr11:129279497-129279746 | Common:3; Rare:109 | ||||
| chr11:129873930-129874196 | Common:1; Rare:93 | ||||
| chr11:129895535-129895663 | Common:2; Rare:47 | ||||
| chr11:130069624-130070049 | Common:2; Rare:153 | ||||
| chr11:130314403-130314467 | Rare:24 | ||||
| chr11:130448401-130448647 | Rare:60 | ||||
| chr11:130916403-130916625 | Common:6; Rare:73 | ||||
| chr11:131911386-131911484 | Common:1; Rare:43 | ||||
| chr11:133532315-133532553 | Common:2; Rare:55 | ||||
| chr11:134223932-134224095 | Common:2; Rare:47 | ||||
| chr11:134253099-134253603 | Common:2; Rare:156; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:134331703-134331990 | Common:10; Rare:60 | ||||
| chr12:389238-389417 | Common:1; Rare:72 |