| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111913141-111913294 | Rare:45 | ||||
| chr11:112025203-112025484 | Common:2; Rare:68; Clinvar:4; Clinvar (benign):3 | ||||
| chr11:112073987-112074092 | Rare:19 | ||||
| chr11:112074172-112074579 | Common:1; Rare:89 | ||||
| chr11:112074669-112074727 | Rare:18 | ||||
| chr11:112086715-112086923 | Rare:89; Clinvar:3; Clinvar (pathogenic):3 | ||||
| chr11:112226233-112226793 | Common:1; Rare:198; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:112227920-112227944 | Rare:2 | ||||
| chr11:112229791-112229893 | Common:2; Rare:24 | ||||
| chr11:113314448-113314608 | Rare:58 | ||||
| chr11:113875469-113875783 | Common:4; Rare:113 | ||||
| chr11:114296062-114296261 | Common:1; Rare:39 | ||||
| chr11:114296266-114296566 | Rare:56 | ||||
| chr11:114400081-114400104 | Rare:15 | ||||
| chr11:114400358-114400765 | Common:2; Rare:149 |