Variant report

Variant	rs118331
Chromosome Location	chr21:39990055-39990056
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]
rs2073427	0.86[MEX][hapmap];1.00[TSI][hapmap]
rs2836546	0.86[CHB][hapmap]
rs460049	0.90[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.94[MEX][hapmap];0.95[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs460439	0.91[ASN][1000 genomes]
rs460667	0.85[MEX][hapmap]
rs462006	1.00[CHB][hapmap];0.90[JPT][hapmap];0.95[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs462179	1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs462317	0.83[AMR][1000 genomes]
rs463226	0.86[AMR][1000 genomes]
rs464484	0.81[CHD][hapmap];0.84[GIH][hapmap];0.82[MEX][hapmap];0.83[AMR][1000 genomes]
rs466939	0.82[CHB][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs467138	0.86[ASN][1000 genomes]
rs73217988	0.93[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:39986800-39990800	Weak transcription	Aorta	Aorta
2	chr21:39989200-39997600	Enhancers	Breast Myoepithelial Primary Cells	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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