| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6481226-6481665 | Common:5; Rare:164 | ||||
| chr11:6481889-6482149 | Common:4; Rare:90 | ||||
| chr11:6603393-6603443 | Common:1; Rare:22 | ||||
| chr11:6603494-6603876 | Common:4; Rare:111; Clinvar (benign):3 | ||||
| chr11:6604007-6604074 | Rare:17 | ||||
| chr11:6607027-6607199 | Rare:51 | ||||
| chr11:6608841-6608924 | Rare:23; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:6611423-6611739 | Common:1; Rare:105 | ||||
| chr11:6612154-6612811 | Common:7; Rare:172; Clinvar:1 | ||||
| chr11:6619193-6619610 | Common:3; Rare:141; Clinvar:4; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chr11:6683013-6683091 | Rare:16 | ||||
| chr11:6683252-6683707 | Common:6; Rare:171 | ||||
| chr11:6926226-6926606 | Common:5; Rare:106 | ||||
| chr11:6926615-6926705 | Common:1; Rare:19 | ||||
| chr11:6926809-6926975 | Common:2; Rare:32 |