| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111923728-111923774 | Common:1; Rare:6 | ||||
| chr11:111937113-111937413 | Common:7; Rare:87 | ||||
| chr11:111988853-111989046 | Rare:36 | ||||
| chr11:112025003-112025152 | Rare:40; Clinvar:2 | ||||
| chr11:112025286-112025482 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:112073995-112074354 | Common:1; Rare:74 | ||||
| chr11:112086709-112086924 | Rare:93; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr11:112226334-112226803 | Common:1; Rare:176; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:112961237-112961655 | Common:4; Rare:192 | ||||
| chr11:113314448-113314602 | Rare:54 | ||||
| chr11:113875454-113875781 | Common:4; Rare:121 | ||||
| chr11:114059410-114059943 | Common:1; Rare:109 | ||||
| chr11:114257642-114257832 | Rare:38 | ||||
| chr11:114400450-114400766 | Common:2; Rare:123 | ||||
| chr11:114440457-114440725 | Rare:67 |