| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:77820532-77821224 | Common:2; Rare:218 | ||||
| chr11:77994639-77994759 | Common:1; Rare:53 | ||||
| chr11:78079713-78079950 | Common:2; Rare:71 | ||||
| chr11:78139563-78139853 | Common:3; Rare:109; Clinvar:2 | ||||
| chr11:78188586-78188953 | Common:3; Rare:114 | ||||
| chr11:78574766-78574979 | Common:2; Rare:82; Clinvar (benign):1 | ||||
| chr11:79021770-79021833 | Rare:11 | ||||
| chr11:82900569-82900900 | Common:2; Rare:79 | ||||
| chr11:83071735-83072135 | Common:4; Rare:112 | ||||
| chr11:83156830-83157271 | Common:3; Rare:138 | ||||
| chr11:83157418-83157694 | Rare:82 | ||||
| chr11:83193604-83193849 | Common:1; Rare:110 | ||||
| chr11:83193881-83194208 | Rare:110 | ||||
| chr11:83285558-83286136 | Common:5; Rare:212 | ||||
| chr11:83286312-83286511 | Rare:50 |