| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46381350-46381761 | Common:3; Rare:90 | ||||
| chr11:46617183-46617600 | Common:5; Rare:118 | ||||
| chr11:46700549-46700769 | Common:1; Rare:55 | ||||
| chr11:46700869-46701068 | Common:3; Rare:43 | ||||
| chr11:46846211-46846422 | Common:1; Rare:61 | ||||
| chr11:47176835-47177126 | Common:1; Rare:121 | ||||
| chr11:47214816-47215110 | Common:2; Rare:72; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47248765-47248963 | Rare:81 | ||||
| chr11:47269614-47269727 | Common:1; Rare:38 | ||||
| chr11:47269986-47270212 | Common:1; Rare:82 | ||||
| chr11:47565499-47565620 | Common:3; Rare:23 | ||||
| chr11:47578940-47579094 | Rare:81; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642473-47642786 | Rare:119 | ||||
| chr11:47715341-47715435 | Common:1; Rare:27 | ||||
| chr11:49208338-49208667 | Common:2; Rare:89 |