Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:29944132-29944615 | Common:37; Rare:121 | ||||
chr6:31720363-31720477 | Common:2; Rare:23 | ||||
chr6:31822061-31822181 | Common:2; Rare:23 | ||||
chr6:32853037-32853099 | Rare:18; Clinvar (benign):1 | ||||
chr6:32894576-32894782 | Common:8; Rare:57 | ||||
chr6:33294709-33294822 | Common:1; Rare:27 | ||||
chr6:35602535-35602594 | Rare:9 | ||||
chr6:35664661-35665016 | Common:1; Rare:46 | ||||
chr6:35687668-35687785 | Rare:23 | ||||
chr6:35731325-35731583 | Common:1; Rare:61 | ||||
chr6:37171061-37171154 | Rare:40 | ||||
chr6:38684372-38684652 | Common:2; Rare:61 | ||||
chr6:42407415-42407641 | Common:1; Rare:41 | ||||
chr6:43624715-43624895 | Common:1; Rare:44 | ||||
chr6:44249412-44249885 | Common:1; Rare:134 |