| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:58578190-58578532 | Common:4; Rare:113 | ||||
| chr11:58578818-58579196 | Common:6; Rare:113 | ||||
| chr11:59142746-59142945 | Common:1; Rare:39 | ||||
| chr11:60906501-60906737 | Rare:63 | ||||
| chr11:60952351-60952570 | Rare:38 | ||||
| chr11:61333014-61333251 | Rare:78 | ||||
| chr11:61361843-61362039 | Common:1; Rare:46 | ||||
| chr11:61362243-61362407 | Common:2; Rare:48; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:61429896-61430144 | Common:1; Rare:106; Clinvar (benign):2 | ||||
| chr11:61792573-61792908 | Common:5; Rare:86 | ||||
| chr11:61967193-61967295 | Rare:33 | ||||
| chr11:61967311-61967760 | Common:3; Rare:166; Clinvar:4 | ||||
| chr11:62545614-62545982 | Common:1; Rare:81 | ||||
| chr11:62591494-62591817 | Rare:106 | ||||
| chr11:62611560-62611841 | Rare:72 |