| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:45847125-45847529 | Common:2; Rare:156 | ||||
| chr11:45917816-45918146 | Common:1; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:46119413-46119544 | Rare:22 | ||||
| chr11:46119811-46119993 | Common:2; Rare:48 | ||||
| chr11:46120949-46121031 | Rare:8 | ||||
| chr11:46121069-46121240 | Common:2; Rare:27 | ||||
| chr11:46345268-46345511 | Common:2; Rare:80 | ||||
| chr11:46617170-46617591 | Common:5; Rare:118 | ||||
| chr11:46700553-46700793 | Common:1; Rare:64 | ||||
| chr11:46700955-46701077 | Common:1; Rare:38 | ||||
| chr11:46846213-46846414 | Common:1; Rare:55 | ||||
| chr11:47176820-47177158 | Common:1; Rare:143 | ||||
| chr11:47214284-47214496 | Common:1; Rare:24 | ||||
| chr11:47214814-47215106 | Common:2; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:47248769-47248938 | Rare:67 |