| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68030353-68030758 | Common:3; Rare:113; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68120691-68120860 | Rare:54 | ||||
| chr11:68121337-68121707 | Common:5; Rare:134 | ||||
| chr11:68212411-68213101 | Common:6; Rare:251 | ||||
| chr11:68213581-68213980 | Common:1; Rare:234 | ||||
| chr11:68271261-68271598 | Common:1; Rare:56 | ||||
| chr11:68271949-68272196 | Common:2; Rare:107 | ||||
| chr11:68312251-68312718 | Common:2; Rare:185; Clinvar (benign):1 | ||||
| chr11:68460536-68460768 | Common:3; Rare:90 | ||||
| chr11:68710351-68710953 | Common:4; Rare:177 | ||||
| chr11:68751420-68751710 | Common:1; Rare:61 | ||||
| chr11:68903779-68904000 | Common:5; Rare:101; Clinvar:4; Clinvar (benign):7 | ||||
| chr11:69048727-69049020 | Common:6; Rare:107 | ||||
| chr11:69640928-69641225 | Rare:62 | ||||
| chr11:69658313-69658462 | Rare:28 |