| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:45665539-45665811 | Common:1; Rare:65 | ||||
| chr11:45804236-45804445 | Common:1; Rare:48 | ||||
| chr11:45804960-45805238 | Common:3; Rare:77; Clinvar:5; Clinvar (benign):1 | ||||
| chr11:45846857-45847090 | Rare:36 | ||||
| chr11:45847123-45847563 | Common:2; Rare:171 | ||||
| chr11:45847567-45847710 | Rare:40 | ||||
| chr11:45917775-45918205 | Common:1; Rare:109; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:45918706-45918875 | Common:1; Rare:41 | ||||
| chr11:45922542-45922740 | Common:5; Rare:63 | ||||
| chr11:46119428-46119629 | Common:1; Rare:43 | ||||
| chr11:46119755-46119863 | Rare:30 | ||||
| chr11:46120032-46120164 | Common:1; Rare:19 | ||||
| chr11:46120464-46120688 | Rare:50 | ||||
| chr11:46120780-46120998 | Rare:40 | ||||
| chr11:46121072-46121702 | Common:2; Rare:141 |