| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:57514600-57514727 | Rare:21 | ||||
| chr11:57514831-57515000 | Rare:34 | ||||
| chr11:57515665-57515843 | Common:1; Rare:33 | ||||
| chr11:57530635-57530952 | Common:2; Rare:75 | ||||
| chr11:57530968-57531103 | Common:1; Rare:23 | ||||
| chr11:57567609-57567988 | Common:2; Rare:100 | ||||
| chr11:57598072-57598256 | Common:1; Rare:55; Clinvar (benign):1 | ||||
| chr11:57657366-57657813 | Common:4; Rare:110 | ||||
| chr11:57667222-57667484 | Common:1; Rare:46 | ||||
| chr11:57667678-57667899 | Common:4; Rare:61 | ||||
| chr11:57667902-57668331 | Common:1; Rare:130 | ||||
| chr11:57668730-57668791 | Rare:12 | ||||
| chr11:57711793-57712045 | Common:1; Rare:76 | ||||
| chr11:57712164-57712680 | Common:9; Rare:178 | ||||
| chr11:57712831-57712863 | Rare:11 |