| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:35619797-35620093 | Common:2; Rare:71 | ||||
| chr11:36510236-36510377 | Rare:40 | ||||
| chr11:43358811-43358954 | Rare:63 | ||||
| chr11:43880690-43880925 | Common:2; Rare:68 | ||||
| chr11:45917824-45918146 | Common:1; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:46120951-46121299 | Common:2; Rare:56 | ||||
| chr11:46617175-46617585 | Common:5; Rare:114 | ||||
| chr11:46700555-46700853 | Common:1; Rare:80 | ||||
| chr11:46700871-46701077 | Common:3; Rare:44 | ||||
| chr11:46846207-46846412 | Common:1; Rare:58 | ||||
| chr11:47214814-47215130 | Common:2; Rare:87; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47269545-47269707 | Common:1; Rare:55 | ||||
| chr11:47269953-47270212 | Common:1; Rare:94 | ||||
| chr11:47565499-47565672 | Common:3; Rare:36 | ||||
| chr11:47578959-47579094 | Rare:69; Clinvar:2; Clinvar (pathogenic):1 |