Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:41966610-41966894 | Common:1; Rare:99 | ||||
chr17:42017346-42017533 | Common:1; Rare:78 | ||||
chr17:42017577-42017814 | Rare:62 | ||||
chr17:42154901-42155279 | Common:4; Rare:102 | ||||
chr17:42422613-42423283 | Common:1; Rare:245; Clinvar:7; Clinvar (pathogenic):2 | ||||
chr17:42458738-42458960 | Common:3; Rare:84 | ||||
chr17:42566888-42567159 | Common:3; Rare:96 | ||||
chr17:42577671-42577864 | Common:1; Rare:96 | ||||
chr17:42609327-42609740 | Common:8; Rare:176; Clinvar (benign):2 | ||||
chr17:42659333-42659464 | Rare:32 | ||||
chr17:42676057-42676181 | Rare:22 | ||||
chr17:42761039-42761382 | Common:2; Rare:98 | ||||
chr17:42798658-42798787 | Rare:43 | ||||
chr17:42833340-42833597 | Common:1; Rare:82 | ||||
chr17:42852488-42852652 | Common:1; Rare:59 |