Variant report

Variant	rs7595556
Chromosome Location	chr2:167758908-167758909
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11888113	1.00[YRI][hapmap];0.87[AMR][1000 genomes]
rs12473079	0.86[AMR][1000 genomes]
rs12473081	0.90[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12478429	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs1355415	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs17614234	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2063437	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4569494	1.00[YRI][hapmap]
rs6709784	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7595607	0.89[AMR][1000 genomes];0.82[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529384	chr2:167143465-167958752	Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:167758800-167759200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr2:167758800-167760200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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