Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:36769497-36769660 | Rare:30 | ||||
chr6:36968033-36968167 | Rare:17 | ||||
chr6:37222093-37222340 | Common:2; Rare:59 | ||||
chr6:40353518-40353690 | Rare:33 | ||||
chr6:42704553-42704816 | Common:3; Rare:77; Clinvar (pathogenic):7 | ||||
chr6:43015237-43015392 | Common:1; Rare:19 | ||||
chr6:43016533-43016793 | Rare:53 | ||||
chr6:43017645-43017965 | Common:1; Rare:69 | ||||
chr6:43172278-43172461 | Common:1; Rare:35 | ||||
chr6:43990720-43990842 | Common:1; Rare:17 | ||||
chr6:44074620-44074755 | Rare:24 | ||||
chr6:44249374-44249858 | Common:1; Rare:131 | ||||
chr6:44251771-44252100 | Common:2; Rare:123 | ||||
chr6:48111131-48111267 | Rare:25 | ||||
chr6:52420912-52421014 | Rare:21 |