| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47848298-47848406 | Common:1; Rare:58 | ||||
| chr11:47848536-47848640 | Common:2; Rare:16 | ||||
| chr11:57335543-57335971 | Common:7; Rare:87 | ||||
| chr11:57338166-57338538 | Common:1; Rare:74 | ||||
| chr11:57426896-57427187 | Common:1; Rare:79 | ||||
| chr11:57514620-57514722 | Rare:18 | ||||
| chr11:57530662-57530949 | Common:2; Rare:73 | ||||
| chr11:57567607-57567731 | Rare:42 | ||||
| chr11:57567863-57567896 | Rare:8 | ||||
| chr11:57567930-57567953 | Rare:4 | ||||
| chr11:57597558-57597708 | Rare:34; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:57657492-57657794 | Common:4; Rare:79 | ||||
| chr11:57667725-57667824 | Common:3; Rare:25 | ||||
| chr11:57712013-57712630 | Common:10; Rare:206 | ||||
| chr11:57741243-57741621 | Common:2; Rare:147 |