| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66856800-66857449 | Common:2; Rare:356 | ||||
| chr11:66957900-66958884 | Common:23; Rare:657; Clinvar:3; Clinvar (benign):3 | ||||
| chr11:67006550-67006860 | Common:2; Rare:72 | ||||
| chr11:67022390-67023615 | Common:16; Rare:616 | ||||
| chr11:67023550-67023980 | Common:1; Rare:109 | ||||
| chr11:67027260-67028160 | Common:5; Rare:175 | ||||
| chr11:67056681-67057010 | Common:3; Rare:205 | ||||
| chr11:67057083-67057745 | Rare:197 | ||||
| chr11:67118852-67119386 | Common:6; Rare:371 | ||||
| chr11:67120274-67120674 | Rare:119 | ||||
| chr11:67120798-67121610 | Common:3; Rare:326 | ||||
| chr11:67239676-67240195 | Common:3; Rare:279 | ||||
| chr11:67240473-67240697 | Rare:45 | ||||
| chr11:67240618-67240861 | Common:1; Rare:56 | ||||
| chr11:67266305-67266652 | Common:4; Rare:147 |