Variant report

Variant	rs1685679
Chromosome Location	chr3:157494084-157494085
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10222405	0.98[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs10446283	0.96[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs10446335	0.98[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs11712832	0.98[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs1552486	0.96[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs1552487	0.98[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs1685680	0.99[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs1872981	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1979578	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1994480	0.97[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs2054862	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7630713	0.99[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs792738	0.99[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs792739	0.94[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs901820	0.85[EUR][1000 genomes]
rs9809803	0.95[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs9836369	0.98[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs9847213	0.98[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs9857956	0.98[AFR][1000 genomes];0.85[EUR][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	nsv592121	chr3:157437068-157593470	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv997770	chr3:157441619-157595315	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:157493000-157494400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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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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