| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43013868-43014276 | Common:2; Rare:90 | ||||
| chr6:43040617-43040925 | Rare:92; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43182091-43182217 | Rare:33 | ||||
| chr6:43516861-43517127 | Common:4; Rare:103; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575892-43576228 | Common:2; Rare:139; Clinvar:8 | ||||
| chr6:43770087-43770221 | Common:2; Rare:40 | ||||
| chr6:44126772-44126919 | Rare:38 | ||||
| chr6:44127342-44127663 | Common:4; Rare:93 | ||||
| chr6:44223468-44223620 | Common:1; Rare:47 | ||||
| chr6:44387276-44387747 | Common:4; Rare:104 | ||||
| chr6:45377866-45378198 | Common:2; Rare:116 | ||||
| chr6:46129777-46130168 | Common:5; Rare:125 | ||||
| chr6:46491964-46492053 | Rare:12 | ||||
| chr6:46652710-46653013 | Rare:77 | ||||
| chr6:46921897-46922053 | Rare:42 |