| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:57712180-57712628 | Common:9; Rare:151 | ||||
| chr11:58575790-58576074 | Common:1; Rare:64 | ||||
| chr11:58578216-58578498 | Common:3; Rare:92 | ||||
| chr11:58905268-58905426 | Common:1; Rare:38 | ||||
| chr11:59142756-59142940 | Common:1; Rare:37 | ||||
| chr11:60914143-60914229 | Rare:24 | ||||
| chr11:61332995-61333259 | Rare:88 | ||||
| chr11:61361775-61362438 | Common:4; Rare:174; Clinvar:11; Clinvar (benign):1 | ||||
| chr11:61429896-61430169 | Common:1; Rare:119; Clinvar:3; Clinvar (benign):5 | ||||
| chr11:61792556-61792988 | Common:6; Rare:127 | ||||
| chr11:61816134-61816396 | Rare:75 | ||||
| chr11:61816519-61816601 | Rare:14 | ||||
| chr11:61816760-61816939 | Rare:54 | ||||
| chr11:61816978-61817016 | Rare:5 | ||||
| chr11:61828225-61828571 | Rare:90 |