| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18526552-18526712 | Common:2; Rare:32 | ||||
| chr11:18526809-18527101 | Common:3; Rare:126 | ||||
| chr11:18527110-18527510 | Common:3; Rare:75 | ||||
| chr11:18588627-18588998 | Common:4; Rare:114 | ||||
| chr11:18634317-18634591 | Common:2; Rare:90 | ||||
| chr11:19117061-19117203 | Common:1; Rare:39 | ||||
| chr11:19240902-19241143 | Rare:75 | ||||
| chr11:19712639-19712840 | Common:2; Rare:75 | ||||
| chr11:19776851-19777369 | Common:6; Rare:253 | ||||
| chr11:19777455-19777855 | Common:3; Rare:132 | ||||
| chr11:20022872-20023026 | Rare:26 | ||||
| chr11:20387341-20387764 | Common:9; Rare:132 | ||||
| chr11:20668851-20669251 | Common:5; Rare:168 | ||||
| chr11:22192840-22193090 | Rare:60 | ||||
| chr11:22625499-22625615 | Rare:57; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 |