Variant report

Variant	rs566188949
Chromosome Location	chr8:129839322-129839323
allele	A/T
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	esv3321643	chr8:129837395-129839943	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv3361425	chr8:129837520-129840218	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:129837200-129839400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr8:129837200-129839600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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

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