| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:57427080-57427219 | Common:1; Rare:40 | ||||
| chr11:57460348-57460749 | Common:2; Rare:89 | ||||
| chr11:57499629-57499806 | Rare:52 | ||||
| chr11:57515686-57515836 | Common:1; Rare:29 | ||||
| chr11:57530598-57530824 | Common:2; Rare:41 | ||||
| chr11:57530958-57531115 | Common:1; Rare:28 | ||||
| chr11:57567613-57567787 | Rare:54 | ||||
| chr11:57568130-57568540 | Common:2; Rare:79 | ||||
| chr11:57597940-57598220 | Common:1; Rare:71 | ||||
| chr11:57598240-57598540 | Common:3; Rare:69; Clinvar (benign):3 | ||||
| chr11:57657417-57657836 | Common:4; Rare:105 | ||||
| chr11:57667222-57667542 | Common:2; Rare:56 | ||||
| chr11:57667688-57668168 | Common:5; Rare:152 | ||||
| chr11:57711804-57711989 | Rare:52 | ||||
| chr11:57712337-57712666 | Common:3; Rare:101 |