Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:36047085-36047296 | Rare:50 | ||||
chr20:36050322-36050684 | Common:2; Rare:128 | ||||
chr20:36545420-36545632 | Common:2; Rare:42 | ||||
chr20:36928683-36928779 | Common:1; Rare:21 | ||||
chr20:36950860-36950910 | Rare:8 | ||||
chr20:41354387-41354709 | Common:1; Rare:81 | ||||
chr20:45898155-45898458 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
chr20:45899093-45899139 | Rare:7 | ||||
chr20:47352502-47352632 | Rare:22 | ||||
chr20:47357800-47357864 | Rare:12 | ||||
chr20:50191285-50191590 | Common:1; Rare:97 | ||||
chr20:50267342-50267506 | Common:4; Rare:34 | ||||
chr20:63690659-63690852 | Rare:78; Clinvar (benign):3 | ||||
chr20:63873485-63873667 | Common:2; Rare:35 | ||||
chr20:63940696-63940823 | Rare:48 |