| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67469212-67469410 | Common:1; Rare:64 | ||||
| chr11:67482901-67483170 | Rare:59; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:67507762-67507884 | Rare:28 | ||||
| chr11:67508181-67508518 | Common:1; Rare:64 | ||||
| chr11:67508678-67508775 | Common:2; Rare:38 | ||||
| chr11:68030393-68030743 | Common:3; Rare:96; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68030891-68030940 | Common:5; Rare:24 | ||||
| chr11:68038925-68039014 | Rare:25; Clinvar:1 | ||||
| chr11:68271891-68272160 | Common:2; Rare:114 | ||||
| chr11:68460223-68460309 | Common:2; Rare:46 | ||||
| chr11:68903779-68903943 | Common:4; Rare:79; Clinvar (benign):6 | ||||
| chr11:69640970-69641418 | Common:1; Rare:111 | ||||
| chr11:69641423-69641511 | Rare:17 | ||||
| chr11:69675309-69675488 | Rare:50 | ||||
| chr11:70398460-70398614 | Common:1; Rare:54 |