| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46617150-46617591 | Common:5; Rare:125 | ||||
| chr11:46700532-46700818 | Common:1; Rare:73 | ||||
| chr11:47168306-47168468 | Common:1; Rare:32 | ||||
| chr11:47171551-47171607 | Rare:15 | ||||
| chr11:47176785-47177193 | Common:1; Rare:172 | ||||
| chr11:47214387-47214674 | Common:1; Rare:36 | ||||
| chr11:47214837-47215110 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47269083-47269727 | Common:4; Rare:162 | ||||
| chr11:47270012-47270172 | Common:1; Rare:56 | ||||
| chr11:47425883-47426163 | Rare:62 | ||||
| chr11:47426193-47426277 | Rare:31 | ||||
| chr11:47426390-47426648 | Common:1; Rare:66 | ||||
| chr11:47565490-47565699 | Common:4; Rare:48 | ||||
| chr11:47578959-47579106 | Rare:74; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642458-47642799 | Rare:123 |