Variant report

Variant	rs58365780
Chromosome Location	chr1:165585430-165585431
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:165584800-165586400	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr1:165585200-165586200	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr1:165585400-165585800	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr1:165585400-165586400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr1:165585400-165586400	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr1:165585400-165586400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr1:165585400-165586400	Enhancers	Stomach Mucosa	stomach
8	chr1:165585400-165586600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr1:165585400-165586800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr1:165585400-165586800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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

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