| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:106022174-106022715 | Common:4; Rare:157 | ||||
| chr11:106076877-106076946 | Rare:10 | ||||
| chr11:106076956-106077122 | Rare:37 | ||||
| chr11:106077234-106077743 | Common:2; Rare:166 | ||||
| chr11:107457315-107457389 | Rare:15 | ||||
| chr11:107457597-107457987 | Common:5; Rare:119 | ||||
| chr11:107565226-107565307 | Common:1; Rare:13 | ||||
| chr11:107565469-107565814 | Rare:93 | ||||
| chr11:107858484-107858919 | Common:2; Rare:138 | ||||
| chr11:107859172-107859496 | Common:1; Rare:59 | ||||
| chr11:107928089-107928481 | Common:3; Rare:94 | ||||
| chr11:108008624-108009055 | Common:1; Rare:101 | ||||
| chr11:108009183-108009425 | Rare:98 | ||||
| chr11:108009651-108009713 | Rare:13 | ||||
| chr11:108121345-108121681 | Common:5; Rare:112; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 |