| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6612172-6612497 | Common:4; Rare:94 | ||||
| chr11:6612589-6612815 | Common:2; Rare:47; Clinvar:1 | ||||
| chr11:6619361-6619560 | Common:3; Rare:66; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr11:6654830-6655590 | Common:6; Rare:173 | ||||
| chr11:6655610-6656080 | Common:4; Rare:99 | ||||
| chr11:6682775-6683274 | Common:3; Rare:250 | ||||
| chr11:6683286-6683688 | Common:6; Rare:142 | ||||
| chr11:6926170-6926620 | Common:5; Rare:124 | ||||
| chr11:7020214-7020655 | Common:1; Rare:129 | ||||
| chr11:7512683-7513874 | Common:10; Rare:268 | ||||
| chr11:7987068-7987360 | Common:8; Rare:113 | ||||
| chr11:8018890-8019260 | Common:2; Rare:106 | ||||
| chr11:8081071-8081228 | Common:2; Rare:41 | ||||
| chr11:8168860-8169330 | Common:6; Rare:156 | ||||
| chr11:8262690-8263878 | Common:15; Rare:416 |