| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:128905949-128906155 | Rare:39 | ||||
| chr11:129435667-129435936 | Common:4; Rare:43 | ||||
| chr11:130002752-130002973 | Common:3; Rare:45 | ||||
| chr11:130002997-130003213 | Common:1; Rare:77 | ||||
| chr11:130314386-130314456 | Rare:27 | ||||
| chr11:130314888-130315014 | Common:2; Rare:40 | ||||
| chr11:130910069-130910367 | Common:1; Rare:90 | ||||
| chr11:130915840-130916011 | Common:1; Rare:56 | ||||
| chr11:131909794-131909949 | Rare:21 | ||||
| chr11:131910457-131910723 | Common:2; Rare:111 | ||||
| chr11:131911116-131911641 | Common:3; Rare:164 | ||||
| chr11:134223909-134224103 | Common:2; Rare:63 | ||||
| chr11:134224537-134224785 | Rare:97 | ||||
| chr11:134225445-134225495 | Rare:14 | ||||
| chr11:134253278-134253606 | Common:2; Rare:118; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 |