| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:74171139-74171363 | Common:1; Rare:75 | ||||
| chr11:74398378-74398556 | Common:3; Rare:39 | ||||
| chr11:74462008-74462314 | Common:2; Rare:48 | ||||
| chr11:74493275-74493369 | Rare:40; Clinvar (pathogenic):1 | ||||
| chr11:74592500-74592688 | Common:1; Rare:64 | ||||
| chr11:74949039-74949385 | Common:6; Rare:108 | ||||
| chr11:75351596-75351888 | Common:3; Rare:86 | ||||
| chr11:75400311-75400403 | Common:1; Rare:27 | ||||
| chr11:75449912-75450061 | Common:1; Rare:48 | ||||
| chr11:75525857-75526005 | Common:2; Rare:40 | ||||
| chr11:75562044-75562303 | Common:1; Rare:64; Clinvar:4; Clinvar (benign):2 | ||||
| chr11:76381118-76381364 | Common:4; Rare:81 | ||||
| chr11:76444651-76444923 | Rare:62 | ||||
| chr11:76444958-76445128 | Common:1; Rare:44 | ||||
| chr11:76669900-76669974 | Rare:14 |