| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:63939246-63939742 | Common:8; Rare:118 | ||||
| chr11:63974120-63974695 | Common:6; Rare:576 | ||||
| chr11:63974867-63975267 | Common:4; Rare:122 | ||||
| chr11:63985705-63986231 | Common:4; Rare:160 | ||||
| chr11:63986288-63986519 | Common:2; Rare:232 | ||||
| chr11:63986442-63987002 | Common:14; Rare:608 | ||||
| chr11:63999561-63999961 | Common:5; Rare:140 | ||||
| chr11:64165494-64166830 | Common:12; Rare:1010 | ||||
| chr11:64185052-64185635 | Common:3; Rare:455 | ||||
| chr11:64185593-64186451 | Common:1; Rare:1350 | ||||
| chr11:64206442-64207012 | Common:5; Rare:359 | ||||
| chr11:64207035-64207471 | Common:4; Rare:241; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr11:64207471-64207852 | Common:4; Rare:428; Clinvar (benign):5 | ||||
| chr11:64207817-64208130 | Common:2; Rare:127 | ||||
| chr11:64225232-64226103 | Common:9; Rare:466 |