| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:128693797-128694273 | Common:2; Rare:96 | ||||
| chr11:128891109-128891532 | Common:13; Rare:116; Clinvar:8 | ||||
| chr11:129279490-129279723 | Common:3; Rare:95 | ||||
| chr11:129895517-129895677 | Common:2; Rare:64 | ||||
| chr11:130002760-130002949 | Common:2; Rare:38 | ||||
| chr11:130002997-130003367 | Common:1; Rare:150 | ||||
| chr11:130069532-130070079 | Common:2; Rare:200 | ||||
| chr11:130314373-130314509 | Common:1; Rare:46 | ||||
| chr11:130448584-130448668 | Rare:21 | ||||
| chr11:130910018-130910299 | Common:1; Rare:81 | ||||
| chr11:130916403-130916613 | Common:4; Rare:72 | ||||
| chr11:134223922-134224115 | Common:2; Rare:58 | ||||
| chr11:134224533-134224706 | Rare:66 | ||||
| chr11:134225441-134225493 | Rare:16 | ||||
| chr11:134253292-134253627 | Common:3; Rare:125; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 |