| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67443419-67443572 | Common:1; Rare:49 | ||||
| chr11:67443809-67443837 | Rare:6 | ||||
| chr11:67482918-67483148 | Rare:50; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:67508033-67508468 | Common:1; Rare:100 | ||||
| chr11:68004046-68004140 | Rare:31 | ||||
| chr11:68030393-68030744 | Common:3; Rare:96; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038915-68039090 | Rare:51; Clinvar:1 | ||||
| chr11:68271862-68272139 | Common:2; Rare:111 | ||||
| chr11:68839306-68839514 | Common:1; Rare:47 | ||||
| chr11:68841798-68842043 | Common:1; Rare:75; Clinvar (benign):2 | ||||
| chr11:68903779-68903943 | Common:4; Rare:79; Clinvar (benign):6 | ||||
| chr11:69640990-69641250 | Common:1; Rare:53 | ||||
| chr11:69675301-69675534 | Common:1; Rare:63 | ||||
| chr11:70398455-70398596 | Common:1; Rare:46 | ||||
| chr11:71448275-71448749 | Common:5; Rare:128; Clinvar:4; Clinvar (benign):1 |