| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47426135-47426294 | Rare:60 | ||||
| chr11:47553054-47553486 | Common:4; Rare:122 | ||||
| chr11:47565420-47565620 | Common:3; Rare:36 | ||||
| chr11:47578932-47579335 | Rare:191; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr11:47642427-47642686 | Rare:107 | ||||
| chr11:47767240-47767666 | Common:2; Rare:140 | ||||
| chr11:47848240-47848394 | Common:1; Rare:78 | ||||
| chr11:47848513-47848640 | Common:3; Rare:21 | ||||
| chr11:47980286-47980611 | Common:2; Rare:111 | ||||
| chr11:48144782-48145081 | Rare:83 | ||||
| chr11:57335778-57335943 | Common:3; Rare:41 | ||||
| chr11:57460605-57460852 | Rare:71 | ||||
| chr11:57530646-57530971 | Common:2; Rare:79 | ||||
| chr11:57567837-57568094 | Common:2; Rare:47 | ||||
| chr11:57711981-57712633 | Common:10; Rare:216 |