| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:57567781-57568154 | Common:2; Rare:79 | ||||
| chr11:57597503-57597722 | Rare:50; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:57649905-57650052 | Common:1; Rare:41 | ||||
| chr11:57667695-57668150 | Common:5; Rare:148 | ||||
| chr11:57712180-57712677 | Common:9; Rare:172 | ||||
| chr11:57741243-57741717 | Common:3; Rare:190 | ||||
| chr11:57761654-57762053 | Common:3; Rare:76 | ||||
| chr11:57781503-57781627 | Rare:16 | ||||
| chr11:58578101-58578104 | Rare:1 | ||||
| chr11:58578121-58578538 | Common:4; Rare:134 | ||||
| chr11:58578886-58579174 | Common:3; Rare:78 | ||||
| chr11:58905834-58906030 | Common:2; Rare:39 | ||||
| chr11:58927429-58927798 | Common:5; Rare:67 | ||||
| chr11:59107016-59107251 | Common:2; Rare:71 | ||||
| chr11:59142547-59142663 | Common:1; Rare:25 |