| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:112025293-112025611 | Common:4; Rare:93; Clinvar:1; Clinvar (benign):6 | ||||
| chr11:112073987-112074356 | Common:1; Rare:78 | ||||
| chr11:112086703-112086921 | Rare:95; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr11:112150929-112151087 | Common:1; Rare:17 | ||||
| chr11:112226314-112226677 | Common:1; Rare:149; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:113314403-113314608 | Rare:73 | ||||
| chr11:113875491-113875775 | Common:4; Rare:103 | ||||
| chr11:114059410-114059797 | Rare:80 | ||||
| chr11:114059816-114060245 | Common:4; Rare:101 | ||||
| chr11:114296103-114296580 | Common:1; Rare:95 | ||||
| chr11:114400451-114400784 | Common:2; Rare:129 | ||||
| chr11:116772912-116773060 | Rare:60 | ||||
| chr11:117144201-117144418 | Common:2; Rare:98 | ||||
| chr11:117178679-117178743 | Rare:26 | ||||
| chr11:117179049-117179180 | Rare:23 |