Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:181261041-181261308 | Rare:86 | ||||
chr6:291984-292382 | Common:1; Rare:69 | ||||
chr6:292413-292541 | Rare:38 | ||||
chr6:693039-693169 | Rare:49 | ||||
chr6:1311946-1312122 | Common:2; Rare:53 | ||||
chr6:2245418-2245825 | Common:1; Rare:136 | ||||
chr6:2971247-2971702 | Common:6; Rare:117 | ||||
chr6:2971744-2971925 | Common:2; Rare:38 | ||||
chr6:2999633-3000018 | Common:10; Rare:80 | ||||
chr6:3068509-3068596 | Common:1; Rare:26 | ||||
chr6:3118589-3118737 | Common:2; Rare:48 | ||||
chr6:3157429-3157662 | Common:6; Rare:79; Clinvar (benign):1 | ||||
chr6:3231730-3231968 | Rare:44 | ||||
chr6:3258825-3259058 | Rare:90 | ||||
chr6:3456020-3456189 | Rare:51 |