| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:64317448-64317638 | Common:3; Rare:69 | ||||
| chr11:64318072-64318218 | Rare:61 | ||||
| chr11:65014032-65014237 | Rare:54 | ||||
| chr11:65084041-65084248 | Common:1; Rare:59 | ||||
| chr11:65181813-65181964 | Rare:30 | ||||
| chr11:65570317-65570483 | Rare:58 | ||||
| chr11:65614216-65614344 | Rare:28 | ||||
| chr11:65662895-65663078 | Common:1; Rare:47 | ||||
| chr11:65872735-65872960 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:66002143-66002522 | Common:3; Rare:102; Clinvar:3; Clinvar (benign):3 | ||||
| chr11:66268323-66268655 | Common:3; Rare:92 | ||||
| chr11:66480239-66480459 | Common:1; Rare:59 | ||||
| chr11:66638393-66638720 | Common:3; Rare:143 | ||||
| chr11:66677775-66678028 | Common:1; Rare:101 | ||||
| chr11:67401789-67402075 | Common:3; Rare:103 |