Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:45891258-45891387 | Common:1; Rare:43; Clinvar:3; Clinvar (benign):1 | ||||
chr20:45934618-45934698 | Rare:43 | ||||
chr20:46364386-46364570 | Common:1; Rare:69 | ||||
chr20:47356693-47356882 | Rare:44 | ||||
chr20:47501698-47501940 | Common:1; Rare:86 | ||||
chr20:49278036-49278239 | Rare:55 | ||||
chr20:50113134-50113229 | Common:5; Rare:45 | ||||
chr20:50958506-50958834 | Common:1; Rare:101; Clinvar (benign):2 | ||||
chr20:56392156-56392687 | Common:6; Rare:141 | ||||
chr20:56468410-56468700 | Rare:103 | ||||
chr20:58515387-58515528 | Common:2; Rare:27 | ||||
chr20:62143307-62143739 | Common:5; Rare:180 | ||||
chr20:62182942-62183049 | Rare:29 | ||||
chr20:62386953-62387126 | Common:3; Rare:76 | ||||
chr20:62937883-62938159 | Common:1; Rare:97 |