Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:75393763-75394059 | Common:1; Rare:65 | ||||
chr17:75456435-75456675 | Common:1; Rare:71 | ||||
chr17:75515444-75515631 | Common:3; Rare:57 | ||||
chr17:75667136-75667411 | Common:4; Rare:95 | ||||
chr17:75784566-75784872 | Common:2; Rare:134 | ||||
chr17:75832996-75833156 | Common:1; Rare:51; Clinvar:1 | ||||
chr17:75855268-75855686 | Common:1; Rare:115 | ||||
chr17:75904860-75905204 | Common:3; Rare:96 | ||||
chr17:75979103-75979299 | Rare:54; Clinvar:4 | ||||
chr17:75979348-75979463 | Common:1; Rare:34; Clinvar (benign):1 | ||||
chr17:76103695-76103867 | Common:5; Rare:60 | ||||
chr17:76353612-76353952 | Common:2; Rare:127 | ||||
chr17:76385274-76385303 | Rare:7 | ||||
chr17:76501354-76501611 | Rare:77; Clinvar (benign):3 | ||||
chr17:76726464-76726886 | Common:5; Rare:161 |