| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47269966-47270166 | Common:1; Rare:64 | ||||
| chr11:47426346-47426648 | Common:1; Rare:75 | ||||
| chr11:47565499-47565688 | Common:3; Rare:42 | ||||
| chr11:47578959-47579114 | Rare:81; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642443-47642721 | Rare:112 | ||||
| chr11:57530703-57530843 | Common:1; Rare:37 | ||||
| chr11:57712039-57712643 | Common:9; Rare:199 | ||||
| chr11:59142667-59142879 | Rare:32 | ||||
| chr11:59668983-59669310 | Rare:113 | ||||
| chr11:60924352-60924557 | Common:2; Rare:64 | ||||
| chr11:61333051-61333266 | Rare:74 | ||||
| chr11:61361874-61361964 | Common:1; Rare:20 | ||||
| chr11:61362243-61362404 | Common:2; Rare:47; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:61429912-61430152 | Common:1; Rare:106; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:61792572-61792975 | Common:5; Rare:111 |