Variant report

Variant	rs2836455
Chromosome Location	chr21:39883631-39883632
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11701364	0.85[CEU][hapmap];0.87[TSI][hapmap];0.80[EUR][1000 genomes]
rs2212598	0.89[EUR][1000 genomes]
rs2836453	1.00[YRI][hapmap]
rs2836463	0.93[CEU][hapmap];0.91[CHB][hapmap];0.84[CHD][hapmap];0.88[TSI][hapmap];0.90[EUR][1000 genomes]
rs2836475	0.86[CEU][hapmap];0.95[CHB][hapmap];0.81[EUR][1000 genomes]
rs3787909	0.85[YRI][hapmap]
rs67297531	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8127366	0.81[CHB][hapmap]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:39879800-39884200	Weak transcription	HUVEC	blood vessel
2	chr21:39880000-39891200	Weak transcription	Aorta	Aorta
3	chr21:39883600-39884000	Enhancers	Breast Myoepithelial Primary Cells	Breast

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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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