| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:75562027-75562141 | Rare:25; Clinvar (benign):1 | ||||
| chr11:75562234-75562339 | Common:1; Rare:27; Clinvar (benign):1 | ||||
| chr11:75562676-75562914 | Common:1; Rare:53 | ||||
| chr11:75563150-75563490 | Rare:61 | ||||
| chr11:75768401-75768545 | Rare:41 | ||||
| chr11:75768676-75768804 | Rare:54 | ||||
| chr11:75815076-75815414 | Common:2; Rare:112 | ||||
| chr11:76381037-76381402 | Common:4; Rare:124 | ||||
| chr11:76444567-76444817 | Rare:71 | ||||
| chr11:76444951-76445108 | Common:1; Rare:41 | ||||
| chr11:76783006-76783370 | Common:9; Rare:116 | ||||
| chr11:76783432-76783576 | Common:2; Rare:29 | ||||
| chr11:76783968-76784152 | Common:4; Rare:45 | ||||
| chr11:76784536-76784859 | Common:6; Rare:78 | ||||
| chr11:76860642-76860983 | Common:4; Rare:112 |