Variant report

Variant	rs2036798
Chromosome Location	chr18:45038760-45038761
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs12607893	0.90[AFR][1000 genomes];0.81[ASN][1000 genomes]
rs1995856	0.83[EUR][1000 genomes]
rs4939659	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4939854	0.82[ASN][1000 genomes]
rs4939862	0.82[ASN][1000 genomes]
rs4939968	0.82[EUR][1000 genomes]
rs7506616	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs8095913	0.83[ASN][1000 genomes]
rs9635948	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:45038200-45038800	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr18:45038200-45040000	Enhancers	Brain Germinal Matrix	brain
3	chr18:45038400-45038800	Enhancers	Brain Hippocampus Middle	brain
4	chr18:45038600-45039000	Enhancers	Brain Substantia Nigra	brain

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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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