Variant report

Variant	rs12613172
Chromosome Location	chr2:167977807-167977808
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10497319	0.82[CHD][hapmap];1.00[GIH][hapmap];1.00[EUR][1000 genomes]
rs12612401	1.00[EUR][1000 genomes]
rs12618221	0.82[CHB][hapmap]
rs12620446	1.00[EUR][1000 genomes]
rs12621191	1.00[EUR][1000 genomes]
rs16853054	1.00[EUR][1000 genomes]
rs16853083	0.82[CHB][hapmap];1.00[EUR][1000 genomes]
rs28562247	1.00[EUR][1000 genomes]
rs57732129	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58783083	1.00[EUR][1000 genomes]
rs59955159	1.00[EUR][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	nsv875376	chr2:167844513-168037489	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 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	chr2:167973000-167978200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr2:167973200-167978000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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