| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:35525581-35525693 | Rare:36 | ||||
| chr11:36510249-36510372 | Rare:33 | ||||
| chr11:43358802-43358979 | Rare:83 | ||||
| chr11:44310022-44310320 | Rare:97; Clinvar:2 | ||||
| chr11:45917816-45917913 | Rare:32 | ||||
| chr11:46120958-46121015 | Rare:5 | ||||
| chr11:46617198-46617572 | Common:5; Rare:107 | ||||
| chr11:46700562-46700842 | Common:1; Rare:71 | ||||
| chr11:46846211-46846414 | Common:1; Rare:56 | ||||
| chr11:47186407-47186542 | Rare:38 | ||||
| chr11:47214840-47215094 | Common:2; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:47269574-47269684 | Common:1; Rare:40 | ||||
| chr11:47270012-47270199 | Common:1; Rare:67 | ||||
| chr11:47426368-47426647 | Common:1; Rare:72 | ||||
| chr11:47565383-47565640 | Common:3; Rare:45 |