| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47269874-47270268 | Common:2; Rare:126 | ||||
| chr11:47377965-47378144 | Common:1; Rare:43 | ||||
| chr11:47378465-47378722 | Rare:50 | ||||
| chr11:47407067-47407173 | Rare:19 | ||||
| chr11:47407953-47408205 | Rare:43 | ||||
| chr11:47408296-47408691 | Common:3; Rare:119; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:47426169-47426284 | Rare:43 | ||||
| chr11:47426406-47426979 | Common:2; Rare:113 | ||||
| chr11:47552648-47552993 | Common:2; Rare:135 | ||||
| chr11:47553051-47553405 | Common:2; Rare:118 | ||||
| chr11:47565368-47565712 | Common:4; Rare:69 | ||||
| chr11:47566118-47566176 | Rare:12 | ||||
| chr11:47578895-47579161 | Rare:131; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642200-47642297 | Rare:24 | ||||
| chr11:47642386-47642923 | Rare:161 |