| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67303356-67303582 | Rare:58 | ||||
| chr11:67317773-67317881 | Rare:20 | ||||
| chr11:67353277-67353309 | Rare:12 | ||||
| chr11:67353473-67353720 | Common:1; Rare:63 | ||||
| chr11:67401743-67402074 | Common:3; Rare:121 | ||||
| chr11:67428336-67428537 | Rare:69 | ||||
| chr11:67443458-67443598 | Common:1; Rare:51 | ||||
| chr11:67482936-67483154 | Rare:50; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:68030393-68030744 | Common:3; Rare:96; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038919-68039101 | Rare:53; Clinvar:1 | ||||
| chr11:68271891-68272134 | Common:2; Rare:103 | ||||
| chr11:68460223-68460329 | Common:2; Rare:52 | ||||
| chr11:68903800-68903938 | Common:4; Rare:61; Clinvar (benign):6 | ||||
| chr11:69640972-69641255 | Common:1; Rare:57 | ||||
| chr11:69675309-69675488 | Rare:50 |