Variant report

Variant	rs59755871
Chromosome Location	chr3:23013407-23013408
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs17340014	0.95[AFR][1000 genomes]
rs57132267	1.00[AMR][1000 genomes]
rs57619655	1.00[AMR][1000 genomes]
rs58331496	0.84[AFR][1000 genomes]
rs59561064	1.00[AMR][1000 genomes]
rs59989113	1.00[AMR][1000 genomes]

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	nsv1014828	chr3:22554271-23033498	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1008306	chr3:22762892-23026548	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:23012800-23013600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr3:23012800-23013600	Enhancers	Primary hematopoietic stem cells	blood
3	chr3:23012800-23013800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr3:23013000-23013600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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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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