| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:1833600-1833743 | Common:1; Rare:25 | ||||
| chr11:1834084-1834537 | Common:1; Rare:99 | ||||
| chr11:1924768-1924891 | Common:1; Rare:46 | ||||
| chr11:2137277-2137452 | Rare:44 | ||||
| chr11:2137725-2137940 | Rare:46 | ||||
| chr11:2139270-2139656 | Common:4; Rare:97 | ||||
| chr11:2270567-2270626 | Rare:13 | ||||
| chr11:2377023-2377363 | Common:4; Rare:110 | ||||
| chr11:2400187-2400569 | Common:4; Rare:129 | ||||
| chr11:2400585-2400898 | Common:6; Rare:82 | ||||
| chr11:2401251-2401370 | Rare:29 | ||||
| chr11:2884556-2884723 | Common:1; Rare:54; Clinvar:4; Clinvar (benign):3 | ||||
| chr11:2885708-2885987 | Rare:88; Clinvar:1 | ||||
| chr11:2889759-2889892 | Common:1; Rare:23 | ||||
| chr11:2902035-2902394 | Common:1; Rare:81 |