| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:108222561-108223163 | Common:1; Rare:197; Clinvar:9; Clinvar (benign):1 | ||||
| chr11:108223260-108223441 | Rare:50 | ||||
| chr11:108467469-108467588 | Rare:45 | ||||
| chr11:108498296-108498470 | Common:2; Rare:52 | ||||
| chr11:110092846-110093170 | Common:4; Rare:109 | ||||
| chr11:110296466-110296889 | Common:3; Rare:174; Clinvar:9 | ||||
| chr11:110296954-110297052 | Rare:22 | ||||
| chr11:110429808-110429960 | Common:2; Rare:41 | ||||
| chr11:110429985-110430305 | Common:5; Rare:78 | ||||
| chr11:111299673-111299735 | Common:2; Rare:13 | ||||
| chr11:111602246-111602570 | Common:1; Rare:109 | ||||
| chr11:111766332-111766433 | Common:1; Rare:63 | ||||
| chr11:111871259-111871367 | Rare:33; Clinvar:1 | ||||
| chr11:111871495-111871642 | Rare:60; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:111878758-111879016 | Common:2; Rare:80 |