| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34052119-34052493 | Common:4; Rare:171 | ||||
| chr11:34105481-34105678 | Common:2; Rare:66 | ||||
| chr11:34438784-34439016 | Common:2; Rare:80; Clinvar (benign):1 | ||||
| chr11:34620933-34621196 | Common:3; Rare:49 | ||||
| chr11:34916311-34916709 | Common:10; Rare:164; Clinvar:6; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35943949-35944121 | Common:2; Rare:61 | ||||
| chr11:36289399-36289505 | Common:1; Rare:41 | ||||
| chr11:36510236-36510372 | Rare:38 | ||||
| chr11:43358861-43358983 | Rare:60 | ||||
| chr11:43880651-43880884 | Common:2; Rare:56 | ||||
| chr11:45804997-45805186 | Common:3; Rare:47; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:45847215-45847514 | Common:2; Rare:125 | ||||
| chr11:46120952-46121029 | Rare:8 | ||||
| chr11:46121054-46121104 | Rare:9 | ||||
| chr11:46121133-46121283 | Common:2; Rare:25 |