| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65553474-65553762 | Common:2; Rare:62; Clinvar (benign):1 | ||||
| chr11:65570271-65570500 | Rare:84 | ||||
| chr11:65575848-65576060 | Common:3; Rare:61 | ||||
| chr11:65591770-65592022 | Common:7; Rare:81 | ||||
| chr11:65614051-65614342 | Rare:71 | ||||
| chr11:65649925-65650191 | Common:2; Rare:78 | ||||
| chr11:65660186-65660467 | Common:1; Rare:72 | ||||
| chr11:65662828-65663086 | Common:1; Rare:66 | ||||
| chr11:65711869-65712045 | Rare:54 | ||||
| chr11:65720468-65720591 | Common:1; Rare:69 | ||||
| chr11:65856996-65857356 | Common:4; Rare:109 | ||||
| chr11:65857631-65857934 | Common:3; Rare:116 | ||||
| chr11:65860171-65860466 | Common:1; Rare:97 | ||||
| chr11:65867056-65867331 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:65872682-65872937 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):2 |