| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:102452619-102452899 | Common:1; Rare:89 | ||||
| chr11:106077326-106077746 | Common:2; Rare:138 | ||||
| chr11:108009273-108009342 | Rare:36 | ||||
| chr11:108121429-108121625 | Common:4; Rare:71; Clinvar:1; Clinvar (benign):5 | ||||
| chr11:108222609-108223120 | Common:1; Rare:160; Clinvar:7; Clinvar (benign):1 | ||||
| chr11:111541232-111541407 | Rare:47 | ||||
| chr11:111766338-111766459 | Common:1; Rare:76 | ||||
| chr11:111871302-111871387 | Rare:32; Clinvar:1 | ||||
| chr11:111879469-111879539 | Rare:24 | ||||
| chr11:112073987-112074349 | Common:1; Rare:76 | ||||
| chr11:112086721-112086905 | Rare:76; Clinvar:1 | ||||
| chr11:112226314-112226452 | Rare:62 | ||||
| chr11:113314410-113314598 | Rare:67 | ||||
| chr11:113875493-113875760 | Common:3; Rare:97 | ||||
| chr11:114400438-114400755 | Common:2; Rare:125 |