Variant report

Variant	rs518882
Chromosome Location	chr3:118120313-118120314
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1850944	0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs480491	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs491796	0.92[ASN][1000 genomes]
rs495761	0.86[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs497009	0.84[ASN][1000 genomes]
rs506192	0.85[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs507145	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs508870	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs523712	0.95[ASN][1000 genomes]
rs531289	0.86[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs557455	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs566574	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs576638	0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:118119000-118120600	Enhancers	Liver	Liver
2	chr3:118120000-118128800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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