Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:50199546-50199954 | Common:7; Rare:134; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr17:50200209-50200271 | Rare:9 | ||||
chr17:50373151-50373235 | Common:2; Rare:39 | ||||
chr17:50426057-50426300 | Common:1; Rare:62 | ||||
chr17:50473705-50473987 | Rare:81 | ||||
chr17:50707976-50708021 | Rare:8 | ||||
chr17:50719452-50719818 | Rare:123 | ||||
chr17:50866343-50866811 | Common:3; Rare:125 | ||||
chr17:51079526-51079653 | Common:1; Rare:33 | ||||
chr17:51120555-51120989 | Rare:165 | ||||
chr17:51153326-51153643 | Common:1; Rare:83 | ||||
chr17:51166274-51166572 | Common:3; Rare:72 | ||||
chr17:51259984-51260789 | Common:4; Rare:324 | ||||
chr17:51260855-51260966 | Common:2; Rare:50 | ||||
chr17:54968595-54968814 | Common:3; Rare:100 |