| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66347630-66347857 | Common:5; Rare:54 | ||||
| chr11:66480239-66480455 | Common:1; Rare:58 | ||||
| chr11:66616394-66616649 | Common:1; Rare:70 | ||||
| chr11:66638393-66638735 | Common:4; Rare:151 | ||||
| chr11:66677784-66678023 | Common:1; Rare:96 | ||||
| chr11:66744632-66744907 | Common:3; Rare:106 | ||||
| chr11:67056762-67056941 | Common:1; Rare:51 | ||||
| chr11:67303350-67303582 | Rare:61 | ||||
| chr11:67317640-67317931 | Rare:68 | ||||
| chr11:67353489-67353721 | Common:1; Rare:62 | ||||
| chr11:67401783-67402076 | Common:3; Rare:109 | ||||
| chr11:67428338-67428537 | Rare:69 | ||||
| chr11:67468187-67468212 | Rare:4 | ||||
| chr11:67468217-67468235 | Common:1; Rare:3 | ||||
| chr11:67482915-67483154 | Rare:54; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 |