| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:96221449-96221681 | Common:1; Rare:45 | ||||
| chr11:96276761-96276810 | Rare:4 | ||||
| chr11:102137772-102137840 | Rare:14 | ||||
| chr11:102176775-102176881 | Common:1; Rare:20 | ||||
| chr11:102177055-102177212 | Rare:32 | ||||
| chr11:102221595-102221949 | Common:6; Rare:70 | ||||
| chr11:102225717-102225952 | Rare:48 | ||||
| chr11:102226119-102226286 | Rare:29 | ||||
| chr11:102234455-102234553 | Common:1; Rare:24 | ||||
| chr11:102269924-102270392 | Common:2; Rare:80 | ||||
| chr11:102295206-102295220 | Rare:2 | ||||
| chr11:102401538-102401934 | Common:3; Rare:116 | ||||
| chr11:102426834-102427066 | Common:1; Rare:66 | ||||
| chr11:102772016-102772210 | Common:1; Rare:49 | ||||
| chr11:102795457-102795835 | Common:2; Rare:91; Clinvar (benign):1 |