| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68030317-68031137 | Common:37; Rare:783; Clinvar:6; Clinvar (benign):11 | ||||
| chr11:68031159-68031559 | Rare:137 | ||||
| chr11:68038844-68039409 | Common:1; Rare:395; Clinvar:5 | ||||
| chr11:68043550-68043900 | Common:1; Rare:247; Clinvar:7; Clinvar (pathogenic):3 | ||||
| chr11:68120542-68120962 | Rare:328 | ||||
| chr11:68121276-68121722 | Common:19; Rare:671 | ||||
| chr11:68121778-68122213 | Common:2; Rare:161 | ||||
| chr11:68212650-68213070 | Common:7; Rare:299 | ||||
| chr11:68213250-68213520 | Common:2; Rare:196 | ||||
| chr11:68213422-68214357 | Common:21; Rare:2191 | ||||
| chr11:68271024-68271779 | Common:3; Rare:174 | ||||
| chr11:68271830-68272565 | Common:14; Rare:981 | ||||
| chr11:68312130-68312871 | Common:10; Rare:565; Clinvar:3; Clinvar (benign):7 | ||||
| chr11:68460009-68460837 | Common:36; Rare:1227 | ||||
| chr11:68684190-68685180 | Common:14; Rare:603; Clinvar:4; Clinvar (benign):4 |