| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:83071715-83072118 | Common:4; Rare:108 | ||||
| chr11:83193617-83193786 | Common:1; Rare:79 | ||||
| chr11:83285915-83286090 | Common:3; Rare:79 | ||||
| chr11:83286324-83286479 | Rare:39 | ||||
| chr11:85628339-85628658 | Common:6; Rare:107 | ||||
| chr11:85647882-85648066 | Common:2; Rare:47; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:85686133-85686392 | Common:2; Rare:54 | ||||
| chr11:86069844-86069943 | Common:1; Rare:18 | ||||
| chr11:86245012-86245250 | Common:1; Rare:102 | ||||
| chr11:87037767-87038043 | Common:3; Rare:129 | ||||
| chr11:88337625-88337894 | Common:4; Rare:128; Clinvar:7; Clinvar (benign):3 | ||||
| chr11:90223015-90223174 | Common:1; Rare:61 | ||||
| chr11:93741381-93741702 | Common:7; Rare:131 | ||||
| chr11:93784194-93784374 | Common:3; Rare:55 | ||||
| chr11:94493789-94494031 | Common:3; Rare:68; Clinvar (benign):1 |