Variant report

Variant	rs1482478
Chromosome Location	chr10:44596130-44596131
allele	A/G
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]
rs2128363	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2624694	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2624695	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2639463	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2802490	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2804029	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2818904	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2818914	0.81[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44592600-44596600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr10:44595000-44597200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr10:44595200-44597000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr10:44596000-44597200	Enhancers	Rectal Smooth Muscle	rectum

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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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