| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33161435-33161657 | Common:6; Rare:60 | ||||
| chr11:33257157-33257501 | Common:3; Rare:111 | ||||
| chr11:33257621-33257811 | Rare:44 | ||||
| chr11:33257814-33257870 | Rare:14 | ||||
| chr11:33258075-33258685 | Common:2; Rare:214 | ||||
| chr11:33736385-33736605 | Common:2; Rare:68 | ||||
| chr11:33774484-33774583 | Common:2; Rare:40 | ||||
| chr11:34051613-34051778 | Rare:70 | ||||
| chr11:34052138-34052428 | Common:4; Rare:135 | ||||
| chr11:34105529-34105743 | Common:2; Rare:72 | ||||
| chr11:34438773-34439061 | Common:2; Rare:95; Clinvar (benign):1 | ||||
| chr11:34916270-34916669 | Common:10; Rare:162; Clinvar:6; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35662689-35663397 | Common:2; Rare:226 | ||||
| chr11:35943942-35944103 | Common:2; Rare:56 | ||||
| chr11:36289393-36289505 | Common:1; Rare:44 |