| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44531772-44531958 | Rare:63 | ||||
| chr20:44651662-44651809 | Common:1; Rare:43; Clinvar (benign):1 | ||||
| chr20:44885391-44885823 | Common:8; Rare:137 | ||||
| chr20:44909943-44910129 | Common:2; Rare:82 | ||||
| chr20:44960345-44960522 | Common:1; Rare:72 | ||||
| chr20:44966370-44966581 | Common:1; Rare:82 | ||||
| chr20:45362919-45363251 | Common:1; Rare:100 | ||||
| chr20:45363357-45363538 | Common:1; Rare:49 | ||||
| chr20:45406519-45406723 | Rare:55 | ||||
| chr20:45415958-45416159 | Rare:53 | ||||
| chr20:45791867-45792030 | Common:2; Rare:61 | ||||
| chr20:45812339-45812803 | Common:5; Rare:138 | ||||
| chr20:45812962-45813180 | Common:2; Rare:35 | ||||
| chr20:45827250-45827547 | Common:1; Rare:49 | ||||
| chr20:45833718-45833892 | Common:4; Rare:47 |