Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:111483156-111483550 | Common:1; Rare:137 | ||||
chr6:112087490-112087684 | Rare:49 | ||||
chr6:127266784-127266920 | Common:1; Rare:57 | ||||
chr6:127343344-127343639 | Common:2; Rare:67 | ||||
chr6:159727020-159727122 | Rare:34 | ||||
chr6:159727347-159727685 | Common:5; Rare:138 | ||||
chr6:159789627-159789947 | Common:2; Rare:108 | ||||
chr6:169701996-169702196 | Common:3; Rare:100 | ||||
chr6:169751594-169751644 | Rare:21; Clinvar (benign):1 | ||||
chr7:2242176-2242226 | Common:2; Rare:35 | ||||
chr7:6009035-6009273 | Common:3; Rare:89; Clinvar:1; Clinvar (benign):12 | ||||
chr7:6484077-6484164 | Rare:55 | ||||
chr7:19117627-19117884 | Common:1; Rare:54 | ||||
chr7:23181849-23182065 | Common:2; Rare:88 | ||||
chr7:26201637-26201798 | Common:1; Rare:88 |