| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111912730-111912739 | Rare:1 | ||||
| chr11:111913138-111913276 | Rare:41 | ||||
| chr11:112073995-112074351 | Common:1; Rare:73 | ||||
| chr11:112086686-112086917 | Rare:103; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr11:112150680-112150739 | Rare:15 | ||||
| chr11:112150823-112150948 | Common:1; Rare:17 | ||||
| chr11:112150960-112151155 | Common:1; Rare:29 | ||||
| chr11:113314454-113314609 | Rare:55 | ||||
| chr11:113875485-113875758 | Common:3; Rare:98 | ||||
| chr11:114059406-114060097 | Common:2; Rare:150 | ||||
| chr11:114064619-114064888 | Common:2; Rare:51 | ||||
| chr11:114180512-114180641 | Common:2; Rare:22 | ||||
| chr11:114296234-114296592 | Rare:69 | ||||
| chr11:114400405-114400734 | Common:2; Rare:131 | ||||
| chr11:114439441-114439657 | Common:2; Rare:84 |