| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:75151318-75151392 | Common:1; Rare:14 | ||||
| chr11:75306684-75306787 | Rare:17 | ||||
| chr11:75351456-75351888 | Common:4; Rare:126 | ||||
| chr11:75525907-75526043 | Common:2; Rare:44 | ||||
| chr11:76381101-76381364 | Common:4; Rare:83 | ||||
| chr11:76444660-76444919 | Rare:58 | ||||
| chr11:76669895-76670014 | Rare:20 | ||||
| chr11:76783042-76783379 | Common:10; Rare:113 | ||||
| chr11:77637591-77637868 | Common:1; Rare:91 | ||||
| chr11:77820924-77821210 | Common:1; Rare:86 | ||||
| chr11:78079643-78079946 | Common:2; Rare:104 | ||||
| chr11:78139590-78139779 | Common:3; Rare:76; Clinvar:2 | ||||
| chr11:78188586-78188953 | Common:3; Rare:114 | ||||
| chr11:78417680-78418045 | Common:3; Rare:147 | ||||
| chr11:78574761-78574972 | Common:2; Rare:85; Clinvar (benign):1 |