| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111359388-111359472 | Rare:12 | ||||
| chr11:111601995-111602156 | Rare:31 | ||||
| chr11:111602258-111602604 | Common:1; Rare:115 | ||||
| chr11:111602789-111603155 | Rare:76 | ||||
| chr11:111765918-111765971 | Rare:10 | ||||
| chr11:111766088-111766166 | Common:2; Rare:25 | ||||
| chr11:111766311-111766533 | Common:2; Rare:117 | ||||
| chr11:111766598-111766911 | Rare:70 | ||||
| chr11:111870935-111871010 | Common:1; Rare:16 | ||||
| chr11:111871116-111871432 | Common:5; Rare:84; Clinvar:1 | ||||
| chr11:111871453-111871655 | Rare:72; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:111878688-111879313 | Common:3; Rare:230 | ||||
| chr11:111879407-111879566 | Common:1; Rare:53 | ||||
| chr11:111879580-111879775 | Common:1; Rare:57 | ||||
| chr11:111918738-111919035 | Common:2; Rare:77 |