| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:236331-236494 | Common:6; Rare:47 | ||||
| chr11:236919-237044 | Common:1; Rare:49 | ||||
| chr11:504844-505141 | Common:4; Rare:74 | ||||
| chr11:506732-506981 | Common:3; Rare:86 | ||||
| chr11:576412-576506 | Rare:33 | ||||
| chr11:695614-695841 | Rare:63 | ||||
| chr11:747284-747493 | Rare:89; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:777463-777602 | Common:1; Rare:62 | ||||
| chr11:832826-833020 | Common:7; Rare:64 | ||||
| chr11:842492-842895 | Common:7; Rare:166 | ||||
| chr11:1838700-1839033 | Common:2; Rare:89; Clinvar:1 | ||||
| chr11:1839997-1840656 | Common:1; Rare:202; Clinvar:3; Clinvar (benign):7 | ||||
| chr11:1919470-1919795 | Rare:86; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:1922613-1922886 | Common:1; Rare:78 | ||||
| chr11:1925077-1925116 | Rare:10 |