Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:58427539-58427811 | Common:1; Rare:41 | ||||
chr2:6913909-6914083 | Rare:28 | ||||
chr2:8583790-8584041 | Common:3; Rare:77 | ||||
chr2:8684943-8685096 | Common:5; Rare:54 | ||||
chr2:9229324-9229459 | Rare:28 | ||||
chr2:11750452-11750714 | Common:3; Rare:49 | ||||
chr2:20438537-20438814 | Rare:52 | ||||
chr2:20447729-20447964 | Rare:71 | ||||
chr2:20448112-20448205 | Rare:26 | ||||
chr2:20448381-20448559 | Common:1; Rare:50 | ||||
chr2:20450939-20451024 | Rare:22 | ||||
chr2:25421000-25421110 | Common:1; Rare:22 | ||||
chr2:26209779-26210014 | Common:1; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
chr2:27022125-27022339 | Common:1; Rare:41 | ||||
chr2:27025179-27025499 | Common:1; Rare:69 |