| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:693050-693176 | Rare:44 | ||||
| chr6:2245438-2245825 | Common:1; Rare:133 | ||||
| chr6:2971524-2971719 | Common:1; Rare:54 | ||||
| chr6:3063716-3063968 | Common:2; Rare:87 | ||||
| chr6:3118365-3118755 | Common:5; Rare:129 | ||||
| chr6:3258868-3259020 | Rare:55 | ||||
| chr6:4021209-4021449 | Rare:107 | ||||
| chr6:5003649-5003843 | Common:5; Rare:61 | ||||
| chr6:5004007-5004126 | Common:1; Rare:53 | ||||
| chr6:5260729-5261025 | Common:2; Rare:93; Clinvar (benign):2 | ||||
| chr6:5261275-5261553 | Common:9; Rare:67 | ||||
| chr6:7108587-7108656 | Rare:24 | ||||
| chr6:7313127-7313396 | Common:4; Rare:98 | ||||
| chr6:7389740-7389892 | Common:1; Rare:46 | ||||
| chr6:8064329-8064581 | Common:4; Rare:81 |