Variant report

Variant	rs568854841
Chromosome Location	chr4:118647399-118647400
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879834	chr4:118532627-118663111	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv879837	chr4:118599194-118650042	Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv523419	chr4:118635598-118652449	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:118646800-118648200	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr4:118647000-118647400	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr4:118647000-118647600	Enhancers	HUES48 Cell Line	embryonic stem cell

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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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