| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62547320-62547403 | Rare:25 | ||||
| chr11:62555545-62555742 | Common:1; Rare:31 | ||||
| chr11:62556195-62556490 | Common:2; Rare:49 | ||||
| chr11:62556565-62556669 | Rare:13 | ||||
| chr11:62573670-62574250 | Rare:189 | ||||
| chr11:62574442-62574590 | Rare:35 | ||||
| chr11:62591405-62591931 | Rare:184 | ||||
| chr11:62599180-62599446 | Rare:65 | ||||
| chr11:62599986-62600216 | Common:1; Rare:44 | ||||
| chr11:62600639-62600907 | Rare:74 | ||||
| chr11:62601194-62601381 | Common:1; Rare:45 | ||||
| chr11:62601454-62601497 | Rare:20 | ||||
| chr11:62601590-62602056 | Common:2; Rare:140 | ||||
| chr11:62611824-62612040 | Rare:41 | ||||
| chr11:62612357-62612862 | Common:5; Rare:153; Clinvar:2; Clinvar (benign):2 |