| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66242938-66243240 | Common:1; Rare:62; Clinvar (benign):2 | ||||
| chr11:67277130-67277314 | Rare:55 | ||||
| chr11:67286886-67287199 | Common:1; Rare:58 | ||||
| chr11:67397291-67397521 | Common:2; Rare:108 | ||||
| chr11:67490760-67490812 | Rare:13; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr11:67805302-67805611 | Common:3; Rare:113 | ||||
| chr11:68002612-68002937 | Common:1; Rare:51 | ||||
| chr11:68040416-68040568 | Rare:33 | ||||
| chr11:68054008-68054250 | Rare:70 | ||||
| chr11:69155358-69155551 | Common:2; Rare:46 | ||||
| chr11:69444732-69444845 | Common:4; Rare:18 | ||||
| chr11:70397592-70397796 | Common:2; Rare:38 | ||||
| chr11:72004037-72004159 | Rare:44 | ||||
| chr11:72004719-72004912 | Rare:54 | ||||
| chr11:72005286-72005538 | Common:1; Rare:53 |