| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44582441-44582620 | Rare:28 | ||||
| chr20:44746178-44746288 | Common:1; Rare:29 | ||||
| chr20:44885440-44885835 | Common:6; Rare:118 | ||||
| chr20:44909974-44910105 | Common:1; Rare:51 | ||||
| chr20:44960366-44960517 | Common:1; Rare:55 | ||||
| chr20:44966370-44966571 | Common:1; Rare:78 | ||||
| chr20:45348397-45348593 | Common:1; Rare:55 | ||||
| chr20:45363357-45363533 | Common:1; Rare:46 | ||||
| chr20:45406541-45406735 | Rare:50 | ||||
| chr20:45416064-45416183 | Rare:48; Clinvar:1 | ||||
| chr20:45469531-45469884 | Common:1; Rare:111 | ||||
| chr20:45791870-45792005 | Common:1; Rare:50 | ||||
| chr20:45857334-45857639 | Common:3; Rare:85 | ||||
| chr20:45891184-45891387 | Common:1; Rare:66; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45910921-45911184 | Common:4; Rare:79 |