Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:45992188-45992397 | Common:1; Rare:71; Clinvar:8; Clinvar (benign):3 | ||||
chr21:46688547-46688797 | Common:1; Rare:36 | ||||
chr22:18068506-18068636 | Common:2; Rare:21 | ||||
chr22:19171615-19171744 | Rare:45 | ||||
chr22:20702621-20702785 | Common:1; Rare:39 | ||||
chr22:21014151-21014444 | Rare:78 | ||||
chr22:21149421-21149706 | Rare:15 | ||||
chr22:21260846-21261103 | Rare:28 | ||||
chr22:21416579-21416714 | Rare:17 | ||||
chr22:21568685-21568712 | Rare:5 | ||||
chr22:22298078-22298206 | Common:2; Rare:47 | ||||
chr22:23402486-23402812 | Common:9; Rare:111 | ||||
chr22:23509546-23509726 | Common:1; Rare:25 | ||||
chr22:25447968-25448196 | Common:5; Rare:84 | ||||
chr22:25762179-25762476 | Common:1; Rare:52 |