Variant report

Variant	rs17167882
Chromosome Location	chr7:96500579-96500580
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:96499200-96501000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:96499400-96501000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr7:96499400-96501000	Enhancers	NHEK	skin
4	chr7:96499400-96501200	Enhancers	HMEC	breast
5	chr7:96499600-96501000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr7:96500200-96501200	Enhancers	Placenta	Placenta
7	chr7:96500400-96500600	Enhancers	Esophagus	oesophagus

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links