Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42154899-42155178 | Common:3; Rare:73 | ||||
chr17:42185727-42185872 | Common:2; Rare:31 | ||||
chr17:42275575-42275987 | Common:1; Rare:63 | ||||
chr17:42276309-42276578 | Rare:105 | ||||
chr17:42388547-42388887 | Common:1; Rare:87 | ||||
chr17:42458719-42458960 | Common:3; Rare:88 | ||||
chr17:42566952-42567258 | Common:4; Rare:102 | ||||
chr17:42577532-42577845 | Rare:139 | ||||
chr17:42609316-42609777 | Common:8; Rare:187; Clinvar (benign):2 | ||||
chr17:42659221-42659475 | Rare:74 | ||||
chr17:42682449-42682609 | Rare:38 | ||||
chr17:42683669-42683822 | Common:1; Rare:26 | ||||
chr17:42773347-42773478 | Rare:37 | ||||
chr17:42798661-42798785 | Rare:40 | ||||
chr17:42833093-42833530 | Rare:124 |