| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:8168970-8169117 | Common:3; Rare:51 | ||||
| chr11:8682628-8683036 | Common:2; Rare:170 | ||||
| chr11:8717851-8718184 | Common:7; Rare:84 | ||||
| chr11:8910914-8911299 | Common:7; Rare:112 | ||||
| chr11:8964366-8964570 | Common:4; Rare:69 | ||||
| chr11:8964913-8965076 | Common:2; Rare:42 | ||||
| chr11:9003996-9004124 | Rare:47 | ||||
| chr11:9460650-9461055 | Common:4; Rare:106 | ||||
| chr11:9663972-9664250 | Common:4; Rare:103 | ||||
| chr11:10304865-10305089 | Common:1; Rare:50 | ||||
| chr11:10450521-10450932 | Common:2; Rare:104 | ||||
| chr11:10455089-10455432 | Common:5; Rare:58; Clinvar:2; Clinvar (benign):6 | ||||
| chr11:10455901-10456368 | Rare:80 | ||||
| chr11:10541122-10541370 | Common:1; Rare:91 | ||||
| chr11:10568446-10568907 | Common:1; Rare:99 |