| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:107805473-107805844 | Common:5; Rare:79 | ||||
| chr11:107840744-107841002 | Common:3; Rare:51 | ||||
| chr11:108009911-108010097 | Common:1; Rare:39 | ||||
| chr11:108074857-108075198 | Common:1; Rare:70 | ||||
| chr11:108103066-108103350 | Common:3; Rare:48 | ||||
| chr11:108103420-108103615 | Common:2; Rare:31 | ||||
| chr11:108112409-108112571 | Rare:34 | ||||
| chr11:108141447-108141688 | Common:1; Rare:49; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:108142140-108142523 | Common:2; Rare:85; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:108147118-108147419 | Common:4; Rare:85; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:108722831-108723154 | Common:1; Rare:96 | ||||
| chr11:108872742-108872955 | Common:2; Rare:38 | ||||
| chr11:110104019-110104129 | Rare:17 | ||||
| chr11:110201977-110202163 | Common:2; Rare:32 | ||||
| chr11:110220580-110220870 | Common:1; Rare:51 |