Variant report

Variant	rs532999143
Chromosome Location	chr8:130674247-130674248
allele	C/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	nsv891446	chr8:130656205-130710638	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv3449871	chr8:130674174-130674416	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130672800-130675800	Weak transcription	Primary hematopoietic stem cells	blood
2	chr8:130673200-130675000	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr8:130674000-130675600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr8:130674000-130675800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr8:130674000-130677800	Weak transcription	K562	blood

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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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