Variant report

Variant	rs546183983
Chromosome Location	chr4:147898321-147898322
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1826357	chr4:147876484-147900981	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv3414195	chr4:147897629-147899274	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:147895000-147898400	Enhancers	Primary hematopoietic stem cells	blood
2	chr4:147895600-147899000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr4:147897600-147898400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr4:147897800-147902600	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr4:147897800-147902800	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr4:147898200-147905800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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