| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:45377775-45378198 | Common:2; Rare:135 | ||||
| chr6:46652793-46653022 | Rare:56 | ||||
| chr6:47477676-47478077 | Common:3; Rare:104; Clinvar:5; Clinvar (benign):4 | ||||
| chr6:47478127-47478247 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:49463167-49463434 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52284676-52285064 | Common:2; Rare:135 | ||||
| chr6:52361969-52362221 | Common:4; Rare:78 | ||||
| chr6:52420108-52420385 | Common:3; Rare:116; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52671031-52671175 | Rare:44 | ||||
| chr6:52909686-52909789 | Rare:22 | ||||
| chr6:52995249-52995817 | Common:4; Rare:232 | ||||
| chr6:53061535-53061633 | Rare:17 | ||||
| chr6:53061635-53061925 | Rare:65 | ||||
| chr6:53065368-53065618 | Common:1; Rare:77 | ||||
| chr6:53065705-53065753 | Rare:14 |