Variant report

Variant	rs4652423
Chromosome Location	chr1:179568829-179568830
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]
rs10733002	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1079292	0.83[EUR][1000 genomes]
rs1999069	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2026014	0.83[EUR][1000 genomes]
rs4391629	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4422967	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4652417	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4652421	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs749960	0.83[EUR][1000 genomes]
rs7514875	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];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	chr1:179568800-179569200	Bivalent Enhancer	Fetal Kidney	kidney

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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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