| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:43312140-43312195 | Rare:15 | ||||
| chr11:43312413-43312558 | Common:2; Rare:42 | ||||
| chr11:43358753-43359086 | Rare:136 | ||||
| chr11:43359135-43359461 | Common:1; Rare:107 | ||||
| chr11:43644128-43644433 | Common:3; Rare:60 | ||||
| chr11:43644732-43644849 | Rare:15 | ||||
| chr11:43680588-43680990 | Common:1; Rare:124 | ||||
| chr11:43681012-43681220 | Common:2; Rare:39 | ||||
| chr11:43681239-43681369 | Rare:22 | ||||
| chr11:43880592-43880967 | Common:2; Rare:96 | ||||
| chr11:44065910-44065972 | Rare:8 | ||||
| chr11:44066038-44066587 | Common:5; Rare:140 | ||||
| chr11:44066751-44066969 | Common:2; Rare:33 | ||||
| chr11:44095620-44095784 | Common:1; Rare:42; Clinvar (benign):2 | ||||
| chr11:44564671-44564949 | Common:2; Rare:47 |