| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61357484-61357613 | Rare:19 | ||||
| chr11:61357624-61357651 | Rare:6 | ||||
| chr11:61361770-61362101 | Common:2; Rare:80; Clinvar:3 | ||||
| chr11:61362143-61362443 | Common:2; Rare:88; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:61392285-61392740 | Common:2; Rare:103; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:61429339-61429597 | Common:2; Rare:79 | ||||
| chr11:61429688-61429814 | Common:1; Rare:41 | ||||
| chr11:61429909-61430204 | Common:2; Rare:132; Clinvar:3; Clinvar (benign):9 | ||||
| chr11:61792059-61792191 | Rare:23 | ||||
| chr11:61792476-61793034 | Common:6; Rare:174 | ||||
| chr11:61814642-61814827 | Common:1; Rare:37 | ||||
| chr11:61815054-61815674 | Common:5; Rare:128 | ||||
| chr11:61816104-61816478 | Rare:109 | ||||
| chr11:61816744-61817243 | Common:2; Rare:114 | ||||
| chr11:61827107-61827181 | Rare:12 |