| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:57741283-57741717 | Common:3; Rare:173 | ||||
| chr11:57761615-57761974 | Common:3; Rare:74 | ||||
| chr11:58575839-58575920 | Common:1; Rare:14 | ||||
| chr11:58577597-58577848 | Rare:41 | ||||
| chr11:58577987-58578239 | Common:1; Rare:72 | ||||
| chr11:58578328-58578508 | Common:2; Rare:66 | ||||
| chr11:58578725-58578863 | Common:2; Rare:46 | ||||
| chr11:59142614-59142951 | Common:1; Rare:65 | ||||
| chr11:59668980-59669369 | Rare:131 | ||||
| chr11:59810666-59810885 | Common:3; Rare:75 | ||||
| chr11:59866390-59866658 | Common:1; Rare:58; Clinvar (pathogenic):1 | ||||
| chr11:60841922-60842120 | Common:2; Rare:74 | ||||
| chr11:60906414-60906823 | Rare:101 | ||||
| chr11:60914051-60914210 | Common:1; Rare:42 | ||||
| chr11:61161402-61161783 | Common:1; Rare:109 |