| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66677765-66678068 | Common:1; Rare:112 | ||||
| chr11:66744628-66744859 | Common:3; Rare:97 | ||||
| chr11:66843359-66843507 | Common:3; Rare:72 | ||||
| chr11:67120961-67121254 | Common:1; Rare:61 | ||||
| chr11:67303343-67303575 | Rare:60 | ||||
| chr11:67317748-67317877 | Rare:22 | ||||
| chr11:67353294-67353353 | Rare:20 | ||||
| chr11:67353434-67353721 | Common:1; Rare:70 | ||||
| chr11:67401730-67402101 | Common:3; Rare:134 | ||||
| chr11:67428394-67428537 | Rare:57 | ||||
| chr11:67438367-67438595 | Common:1; Rare:90 | ||||
| chr11:67443403-67443628 | Common:2; Rare:84 | ||||
| chr11:67482915-67483211 | Rare:72; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr11:67507820-67508446 | Common:1; Rare:156 | ||||
| chr11:67508606-67508778 | Common:3; Rare:56 |