Variant report

Variant	rs2896967
Chromosome Location	chr8:34342819-34342820
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10099045	0.89[EUR][1000 genomes]
rs10100459	0.89[EUR][1000 genomes]
rs1445184	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs16882360	0.98[ASN][1000 genomes]
rs1822864	0.98[ASN][1000 genomes]
rs2044355	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2166231	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28366982	0.98[ASN][1000 genomes]
rs4400387	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs4534132	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs6468265	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs66892402	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6991355	0.98[ASN][1000 genomes]
rs7816886	0.84[EUR][1000 genomes]
rs7827353	0.98[ASN][1000 genomes]
rs7833514	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7834257	0.84[EUR][1000 genomes]
rs7836137	0.84[EUR][1000 genomes]
rs9297220	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[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	nsv6147	chr8:34314029-34359124	Weak transcription Enhancers	Chromatin interactive region	2 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	chr8:34340200-34343800	Weak transcription	Fetal Kidney	kidney
2	chr8:34342800-34343800	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr8:34342800-34344600	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr8:34342800-34345000	Enhancers	HUES64 Cell Line	embryonic stem cell

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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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