| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6234618-6234793 | Common:2; Rare:54 | ||||
| chr11:6319745-6319993 | Rare:67 | ||||
| chr11:6320479-6320552 | Common:2; Rare:30 | ||||
| chr11:6390221-6390576 | Common:3; Rare:108; Clinvar (benign):1 | ||||
| chr11:6473871-6474124 | Rare:80 | ||||
| chr11:6481292-6481581 | Common:5; Rare:130 | ||||
| chr11:6603524-6603876 | Common:4; Rare:102; Clinvar (benign):3 | ||||
| chr11:6604007-6604103 | Common:1; Rare:25 | ||||
| chr11:6612250-6612332 | Common:2; Rare:26 | ||||
| chr11:6612479-6612508 | Rare:7 | ||||
| chr11:6612642-6612815 | Common:2; Rare:36; Clinvar:1 | ||||
| chr11:6619405-6619562 | Common:2; Rare:47; Clinvar:1; Clinvar (benign):5 | ||||
| chr11:6682963-6683081 | Rare:23 | ||||
| chr11:6683261-6683662 | Common:6; Rare:150 | ||||
| chr11:7020301-7020651 | Common:1; Rare:114 |