| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66058917-66059338 | Common:1; Rare:95 | ||||
| chr11:66257602-66257820 | Rare:60 | ||||
| chr11:66258397-66258678 | Rare:78 | ||||
| chr11:66268394-66268682 | Common:3; Rare:87 | ||||
| chr11:66288987-66289418 | Common:1; Rare:112 | ||||
| chr11:66344976-66345216 | Common:1; Rare:64 | ||||
| chr11:66347557-66347930 | Common:6; Rare:90; Clinvar (benign):1 | ||||
| chr11:66348088-66348116 | Rare:14 | ||||
| chr11:66371660-66372061 | Common:2; Rare:106 | ||||
| chr11:66480220-66480456 | Common:3; Rare:64 | ||||
| chr11:66491610-66491742 | Rare:54 | ||||
| chr11:66492807-66493149 | Common:1; Rare:91 | ||||
| chr11:66510871-66511089 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr11:66593087-66593253 | Common:1; Rare:61 | ||||
| chr11:66616422-66616661 | Common:1; Rare:69 |