Variant report

Variant	rs72706766
Chromosome Location	chr1:179632536-179632537
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10798697	0.83[ASN][1000 genomes]
rs10913830	0.83[ASN][1000 genomes]
rs11805051	0.83[ASN][1000 genomes]
rs12032339	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12047528	0.87[ASN][1000 genomes]
rs12565489	0.88[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs4133262	0.87[ASN][1000 genomes]
rs72706715	0.83[ASN][1000 genomes]
rs72706717	0.83[ASN][1000 genomes]
rs72706762	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72706786	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8179491	1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179632200-179634000	Enhancers	HUVEC	blood vessel

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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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