| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:45917815-45917918 | Rare:33 | ||||
| chr11:45918105-45918162 | Rare:11 | ||||
| chr11:46120952-46121036 | Rare:8 | ||||
| chr11:46594001-46594111 | Common:1; Rare:23 | ||||
| chr11:46617140-46617590 | Common:5; Rare:126 | ||||
| chr11:46700555-46700818 | Common:1; Rare:68 | ||||
| chr11:46701013-46701074 | Rare:26 | ||||
| chr11:46846178-46846434 | Common:1; Rare:76 | ||||
| chr11:47176846-47177075 | Rare:93 | ||||
| chr11:47186365-47186536 | Rare:51 | ||||
| chr11:47214816-47215115 | Common:2; Rare:74; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47248782-47248957 | Rare:73 | ||||
| chr11:47269525-47269823 | Common:1; Rare:103 | ||||
| chr11:47269966-47270193 | Common:1; Rare:75 | ||||
| chr11:47426402-47426642 | Common:1; Rare:61 |