| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:108222556-108223128 | Common:1; Rare:188; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:110092840-110093163 | Common:4; Rare:107 | ||||
| chr11:110296488-110296750 | Common:1; Rare:124; Clinvar:8 | ||||
| chr11:110712293-110712563 | Common:2; Rare:104 | ||||
| chr11:110712677-110712901 | Common:1; Rare:56 | ||||
| chr11:111602226-111602575 | Common:1; Rare:114 | ||||
| chr11:111766348-111766420 | Rare:38 | ||||
| chr11:111871275-111871387 | Rare:37; Clinvar:1 | ||||
| chr11:111878878-111878981 | Common:2; Rare:36 | ||||
| chr11:111879152-111879541 | Rare:117 | ||||
| chr11:111912611-111912779 | Common:1; Rare:36 | ||||
| chr11:111913142-111913256 | Rare:37 | ||||
| chr11:111937086-111937439 | Common:7; Rare:100 | ||||
| chr11:112025293-112025482 | Common:2; Rare:44; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:112073987-112074351 | Common:1; Rare:77 |