| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43635740-43635873 | Common:1; Rare:32 | ||||
| chr6:43644992-43645105 | Common:1; Rare:35; Clinvar (benign):1 | ||||
| chr6:43687757-43687822 | Common:1; Rare:26 | ||||
| chr6:43770081-43770221 | Common:2; Rare:42 | ||||
| chr6:44127361-44127677 | Common:4; Rare:93 | ||||
| chr6:44246893-44247194 | Common:4; Rare:126 | ||||
| chr6:44387439-44387753 | Common:4; Rare:84 | ||||
| chr6:45377855-45378221 | Common:2; Rare:122 | ||||
| chr6:46129793-46130103 | Common:5; Rare:100 | ||||
| chr6:46170969-46171131 | Rare:40 | ||||
| chr6:46652718-46653040 | Rare:79 | ||||
| chr6:46921905-46922080 | Rare:47 | ||||
| chr6:47478123-47478247 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:49463174-49463401 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52671049-52671175 | Rare:39 |