Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:45791890-45792026 | Common:1; Rare:57 | ||||
chr20:45857326-45857632 | Common:3; Rare:83 | ||||
chr20:45891020-45891448 | Common:3; Rare:123; Clinvar:8; Clinvar (benign):3 | ||||
chr20:45910950-45911184 | Common:4; Rare:72 | ||||
chr20:45934674-45934731 | Rare:24 | ||||
chr20:46008732-46008918 | Common:3; Rare:40 | ||||
chr20:46513527-46513602 | Common:1; Rare:26 | ||||
chr20:47319034-47319184 | Common:1; Rare:53 | ||||
chr20:47356664-47356872 | Rare:45 | ||||
chr20:47501752-47502015 | Common:1; Rare:92 | ||||
chr20:49219217-49219491 | Common:1; Rare:122 | ||||
chr20:49278029-49278291 | Rare:72 | ||||
chr20:49278458-49278717 | Common:9; Rare:100 | ||||
chr20:49915471-49915697 | Common:3; Rare:75 | ||||
chr20:50113112-50113239 | Common:5; Rare:61 |