Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:41688635-41688917 | Common:1; Rare:97 | ||||
chr17:41689301-41689864 | Common:3; Rare:184 | ||||
chr17:41786642-41786850 | Common:3; Rare:58; Clinvar (benign):1 | ||||
chr17:41812620-41813029 | Common:3; Rare:91; Clinvar:5 | ||||
chr17:41918884-41919220 | Common:1; Rare:135; Clinvar:1 | ||||
chr17:41966608-41966837 | Common:1; Rare:83 | ||||
chr17:42017382-42017483 | Rare:46 | ||||
chr17:42017577-42017701 | Rare:37 | ||||
chr17:42154937-42155270 | Common:4; Rare:86 | ||||
chr17:42423153-42423404 | Common:1; Rare:66; Clinvar:1 | ||||
chr17:42458805-42458926 | Common:1; Rare:35 | ||||
chr17:42566992-42567149 | Common:3; Rare:50 | ||||
chr17:42577651-42577864 | Common:1; Rare:103 | ||||
chr17:42609330-42609740 | Common:8; Rare:172; Clinvar (benign):2 | ||||
chr17:42659149-42659421 | Rare:84 |