| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:94973409-94973745 | Rare:93 | ||||
| chr11:95066908-95066952 | Rare:7 | ||||
| chr11:95089737-95089872 | Common:3; Rare:53 | ||||
| chr11:95790369-95790603 | Common:1; Rare:85 | ||||
| chr11:96389857-96390050 | Common:1; Rare:80 | ||||
| chr11:103091831-103091960 | Rare:45 | ||||
| chr11:106077335-106077707 | Common:2; Rare:113 | ||||
| chr11:108009259-108009359 | Rare:48 | ||||
| chr11:108222614-108223127 | Common:1; Rare:159; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:111879161-111879500 | Rare:97 | ||||
| chr11:111911938-111912128 | Common:3; Rare:39 | ||||
| chr11:111912586-111912905 | Common:1; Rare:78 | ||||
| chr11:111913132-111913532 | Common:1; Rare:106 | ||||
| chr11:112073995-112074351 | Common:1; Rare:73 | ||||
| chr11:112086709-112086910 | Rare:85; Clinvar:1; Clinvar (pathogenic):1 |