| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18268431-18268742 | Common:2; Rare:80 | ||||
| chr11:18384174-18384354 | Rare:37 | ||||
| chr11:18384421-18384508 | Common:1; Rare:12 | ||||
| chr11:18384746-18384840 | Rare:12 | ||||
| chr11:18633289-18633514 | Rare:39 | ||||
| chr11:18768471-18768750 | Rare:45 | ||||
| chr11:19432528-19432843 | Common:2; Rare:48 | ||||
| chr11:19776788-19777009 | Rare:50 | ||||
| chr11:19777052-19777131 | Common:2; Rare:34 | ||||
| chr11:22193677-22193715 | Rare:18 | ||||
| chr11:22624827-22625086 | Common:3; Rare:85; Clinvar:7; Clinvar (benign):5 | ||||
| chr11:22657270-22657482 | Rare:33 | ||||
| chr11:23078447-23078470 | Rare:7 | ||||
| chr11:26087661-26087767 | Common:2; Rare:19 | ||||
| chr11:27212392-27212659 | Rare:38 |