Variant report

Variant	rs2836461
Chromosome Location	chr21:39895598-39895599
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11909285	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17193990	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2836457	1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2836460	1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2836462	1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2836465	0.91[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2836467	1.00[JPT][hapmap];0.91[YRI][hapmap];0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2836468	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs2836470	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs2836524	1.00[CHB][hapmap]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:39892000-39896000	Enhancers	HepG2	liver
2	chr21:39892600-39896000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr21:39893600-39896400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr21:39895400-39895800	Enhancers	Aorta	Aorta
5	chr21:39895400-39896200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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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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