| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66510547-66510677 | Common:1; Rare:59; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr11:66593042-66593223 | Common:1; Rare:67 | ||||
| chr11:66616383-66616661 | Common:1; Rare:86 | ||||
| chr11:66638417-66638740 | Common:4; Rare:140 | ||||
| chr11:66677769-66678128 | Common:1; Rare:126 | ||||
| chr11:66744623-66744883 | Common:3; Rare:108 | ||||
| chr11:66958522-66958833 | Common:5; Rare:80 | ||||
| chr11:67239819-67240170 | Rare:74 | ||||
| chr11:67317767-67317877 | Rare:19 | ||||
| chr11:67353523-67353811 | Common:2; Rare:81 | ||||
| chr11:67401783-67402076 | Common:3; Rare:109 | ||||
| chr11:67428244-67428585 | Common:1; Rare:120 | ||||
| chr11:67443445-67443697 | Common:2; Rare:84 | ||||
| chr11:67469228-67469356 | Rare:38 | ||||
| chr11:67482941-67483192 | Rare:56; Clinvar:2; Clinvar (benign):3 |