| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34632559-34632578 | Rare:3 | ||||
| chr11:34642667-34642957 | Common:2; Rare:69 | ||||
| chr11:34916102-34916734 | Common:16; Rare:244; Clinvar:8; Clinvar (benign):17; Clinvar (pathogenic):1 | ||||
| chr11:35139018-35139369 | Common:1; Rare:96 | ||||
| chr11:35662817-35663126 | Rare:97 | ||||
| chr11:35943886-35944131 | Common:3; Rare:80 | ||||
| chr11:36510214-36510377 | Rare:53 | ||||
| chr11:43358849-43358983 | Rare:64 | ||||
| chr11:43680581-43680870 | Rare:89 | ||||
| chr11:43880735-43880863 | Common:1; Rare:23 | ||||
| chr11:44066001-44066555 | Common:5; Rare:142 | ||||
| chr11:45181537-45181764 | Common:1; Rare:51 | ||||
| chr11:45804265-45804527 | Common:1; Rare:52 | ||||
| chr11:45804974-45805175 | Common:3; Rare:47; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:45847190-45847503 | Common:2; Rare:129 |