| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:44387445-44387789 | Common:4; Rare:92 | ||||
| chr6:45328137-45328487 | Rare:107; Clinvar (benign):1 | ||||
| chr6:45377855-45378189 | Common:2; Rare:114 | ||||
| chr6:50818841-50818871 | Common:1; Rare:5; Clinvar (benign):1 | ||||
| chr6:50818873-50818932 | Rare:17 | ||||
| chr6:52284676-52285027 | Common:2; Rare:124 | ||||
| chr6:52670969-52671161 | Rare:61 | ||||
| chr6:52995267-52995817 | Common:4; Rare:228 | ||||
| chr6:53065336-53065596 | Common:1; Rare:85 | ||||
| chr6:53348902-53349222 | Common:2; Rare:115 | ||||
| chr6:55875512-55875712 | Rare:36 | ||||
| chr6:56091614-56091695 | Rare:8 | ||||
| chr6:56542795-56543131 | Common:2; Rare:59 | ||||
| chr6:57046503-57046747 | Rare:86 | ||||
| chr6:57089885-57090227 | Rare:125 |