| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46846218-46846415 | Common:1; Rare:55 | ||||
| chr11:47176842-47177131 | Common:1; Rare:118 | ||||
| chr11:47186367-47186529 | Rare:49 | ||||
| chr11:47214840-47215084 | Common:2; Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:47248794-47248941 | Rare:57 | ||||
| chr11:47269545-47269700 | Common:1; Rare:51 | ||||
| chr11:47269974-47270184 | Common:1; Rare:69 | ||||
| chr11:47408355-47408628 | Rare:89 | ||||
| chr11:47426363-47426648 | Common:1; Rare:73 | ||||
| chr11:47449043-47449240 | Rare:47; Clinvar:5; Clinvar (pathogenic):1 | ||||
| chr11:47553045-47553458 | Common:3; Rare:123 | ||||
| chr11:47565368-47565712 | Common:4; Rare:69 | ||||
| chr11:47578920-47579097 | Rare:91; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642466-47642824 | Rare:131 | ||||
| chr11:47848305-47848419 | Rare:63 |