| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6390162-6390495 | Common:2; Rare:91 | ||||
| chr11:6405362-6405606 | Common:1; Rare:49 | ||||
| chr11:6418997-6419178 | Common:2; Rare:39 | ||||
| chr11:6419387-6419489 | Rare:33 | ||||
| chr11:6457840-6458133 | Common:1; Rare:69 | ||||
| chr11:6473844-6474107 | Rare:84 | ||||
| chr11:6481276-6481585 | Common:5; Rare:133 | ||||
| chr11:6603524-6603806 | Common:4; Rare:84 | ||||
| chr11:6612642-6612706 | Common:1; Rare:13 | ||||
| chr11:6619371-6619541 | Common:2; Rare:58; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr11:6656232-6656851 | Common:1; Rare:102 | ||||
| chr11:6683249-6683656 | Common:6; Rare:155 | ||||
| chr11:7020301-7020519 | Rare:77 | ||||
| chr11:8018936-8019283 | Common:2; Rare:100 | ||||
| chr11:8038455-8038813 | Common:2; Rare:95 |