| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:19712512-19712887 | Common:2; Rare:131 | ||||
| chr11:19777660-19777851 | Common:1; Rare:47 | ||||
| chr11:20022943-20023029 | Rare:14 | ||||
| chr11:20023203-20023366 | Rare:30 | ||||
| chr11:20027375-20027525 | Common:3; Rare:41 | ||||
| chr11:20027695-20027894 | Common:1; Rare:33 | ||||
| chr11:20363624-20363818 | Common:4; Rare:37 | ||||
| chr11:20364000-20364214 | Common:6; Rare:45 | ||||
| chr11:20387147-20387776 | Common:10; Rare:180 | ||||
| chr11:20388131-20388276 | Rare:51 | ||||
| chr11:22624937-22625372 | Common:4; Rare:163; Clinvar:12; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr11:22625375-22625671 | Common:3; Rare:140; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr11:22625675-22626098 | Common:4; Rare:144; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr11:22674659-22674931 | Common:3; Rare:48 | ||||
| chr11:22829262-22829437 | Common:1; Rare:48 |