Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:63944697-63944793 | Rare:28 | ||||
chr21:14027267-14027490 | Common:4; Rare:67 | ||||
chr21:16194265-16194585 | Common:2; Rare:89 | ||||
chr21:16588498-16588762 | Common:1; Rare:61 | ||||
chr21:26965492-26965750 | Common:2; Rare:108 | ||||
chr21:26967084-26967153 | Rare:11 | ||||
chr21:29002716-29002811 | Common:1; Rare:34 | ||||
chr21:31667159-31667298 | Rare:33; Clinvar:1; Clinvar (pathogenic):3 | ||||
chr21:32325283-32325486 | Rare:62 | ||||
chr21:34836720-34836849 | Common:1; Rare:20 | ||||
chr21:34854020-34854420 | Common:1; Rare:73 | ||||
chr21:34888107-34888154 | Common:1; Rare:7 | ||||
chr21:36320799-36320820 | Rare:9 | ||||
chr21:37221314-37221438 | Common:1; Rare:53 | ||||
chr21:38907266-38907447 | Rare:38 |