| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:292430-292536 | Rare:32 | ||||
| chr6:693069-693188 | Rare:38 | ||||
| chr6:2999644-2999917 | Common:10; Rare:59 | ||||
| chr6:3118584-3118741 | Common:2; Rare:51 | ||||
| chr6:3157459-3157676 | Common:6; Rare:80 | ||||
| chr6:3227509-3227977 | Rare:113 | ||||
| chr6:3231730-3231886 | Rare:25 | ||||
| chr6:3258825-3259025 | Rare:77 | ||||
| chr6:3455988-3456007 | Rare:5 | ||||
| chr6:3456038-3456171 | Rare:43 | ||||
| chr6:3849239-3849414 | Common:2; Rare:50 | ||||
| chr6:4021209-4021423 | Rare:99 | ||||
| chr6:5004007-5004115 | Common:1; Rare:52 | ||||
| chr6:5260677-5261059 | Common:5; Rare:137; Clinvar (benign):4 | ||||
| chr6:5261276-5261553 | Common:9; Rare:67 |