| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66438736-66439153 | Common:2; Rare:110 | ||||
| chr11:66466679-66466956 | Rare:84 | ||||
| chr11:66480212-66480465 | Common:3; Rare:69 | ||||
| chr11:66510547-66510687 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr11:66593036-66593209 | Common:1; Rare:61 | ||||
| chr11:66616396-66616661 | Common:1; Rare:78 | ||||
| chr11:66638393-66638747 | Common:4; Rare:156 | ||||
| chr11:66677769-66678125 | Common:1; Rare:126 | ||||
| chr11:66744632-66744838 | Common:1; Rare:84 | ||||
| chr11:66843320-66843448 | Common:5; Rare:66 | ||||
| chr11:67056784-67056923 | Common:1; Rare:42 | ||||
| chr11:67239781-67240134 | Common:1; Rare:72 | ||||
| chr11:67303158-67303569 | Common:3; Rare:95 | ||||
| chr11:67317698-67317886 | Rare:42 | ||||
| chr11:67353504-67353625 | Rare:33 |