| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:22625530-22625609 | Rare:39; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625808-22626002 | Common:2; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:24496771-24497231 | Common:4; Rare:120 | ||||
| chr11:27363022-27363306 | Common:1; Rare:126 | ||||
| chr11:27506716-27506877 | Common:1; Rare:75 | ||||
| chr11:28108120-28108414 | Common:1; Rare:89 | ||||
| chr11:30016943-30017136 | Rare:53 | ||||
| chr11:30322971-30323195 | Common:2; Rare:64 | ||||
| chr11:30584029-30584130 | Rare:26 | ||||
| chr11:31369724-31369936 | Rare:65 | ||||
| chr11:31509526-31509949 | Common:2; Rare:154 | ||||
| chr11:31810970-31811375 | Rare:64; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:31811684-31811787 | Rare:30 | ||||
| chr11:31812164-31812406 | Common:5; Rare:46 | ||||
| chr11:31812508-31812605 | Rare:11 |