| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:60952519-60952818 | Rare:51 | ||||
| chr11:61161085-61161349 | Rare:61 | ||||
| chr11:61161358-61161888 | Common:1; Rare:145 | ||||
| chr11:61294720-61295002 | Rare:64 | ||||
| chr11:61295224-61295471 | Common:1; Rare:56 | ||||
| chr11:61332999-61333394 | Common:1; Rare:144 | ||||
| chr11:61356780-61356958 | Common:1; Rare:32 | ||||
| chr11:61357294-61357580 | Common:1; Rare:37 | ||||
| chr11:61357588-61357688 | Rare:19 | ||||
| chr11:61361780-61362468 | Common:4; Rare:183; Clinvar:11; Clinvar (benign):1 | ||||
| chr11:61392341-61392886 | Common:2; Rare:121; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:61429353-61429630 | Common:2; Rare:84 | ||||
| chr11:61429903-61430285 | Common:2; Rare:157; Clinvar:3; Clinvar (benign):9 | ||||
| chr11:61430346-61430381 | Rare:8 | ||||
| chr11:61791990-61792190 | Rare:39 |