Variant report

Variant	rs73131595
Chromosome Location	chr5:91605448-91605449
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs4485908	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60047729	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60899707	1.00[AMR][1000 genomes]
rs73129459	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73129478	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73133057	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73133062	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73133075	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73133077	1.00[AMR][1000 genomes]
rs73133079	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73134921	1.00[AMR][1000 genomes]
rs73134929	1.00[AMR][1000 genomes]
rs73134939	1.00[AMR][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:91604000-91606000	Enhancers	A549	lung
2	chr5:91604000-91607200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr5:91604000-91607200	Enhancers	Fetal Heart	heart
4	chr5:91604200-91606400	Enhancers	Muscle Satellite Cultured Cells	--
5	chr5:91604400-91606600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr5:91604600-91605800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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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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