| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:36224102-36224493 | Common:1; Rare:123 | ||||
| chr1:36450423-36450601 | Common:1; Rare:54 | ||||
| chr1:36464247-36464468 | Common:2; Rare:61 | ||||
| chr1:37474384-37474587 | Common:1; Rare:79 | ||||
| chr1:37561420-37561654 | Common:1; Rare:65 | ||||
| chr1:37595888-37596038 | Common:1; Rare:51 | ||||
| chr1:37692219-37692578 | Common:4; Rare:84 | ||||
| chr1:37859550-37859784 | Common:3; Rare:78 | ||||
| chr1:37989961-37990097 | Rare:56 | ||||
| chr1:38859686-38860028 | Rare:132 | ||||
| chr1:38873304-38873563 | Common:3; Rare:92 | ||||
| chr1:39026238-39026397 | Common:1; Rare:42 | ||||
| chr1:39414093-39414342 | Common:1; Rare:75 | ||||
| chr1:39738762-39738930 | Common:1; Rare:41 | ||||
| chr1:39883431-39883570 | Common:1; Rare:58; Clinvar (pathogenic):1 |