Variant report

Variant	rs7570466
Chromosome Location	chr2:180486188-180486189
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]
rs10196048	1.00[JPT][hapmap]
rs10497543	1.00[JPT][hapmap]
rs10930882	1.00[JPT][hapmap]
rs11690551	1.00[JPT][hapmap]
rs11904349	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12614173	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1399689	1.00[JPT][hapmap]
rs1515268	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1515292	1.00[JPT][hapmap]
rs1877944	1.00[JPT][hapmap]
rs2138193	0.81[EUR][1000 genomes]
rs7608208	0.83[EUR][1000 genomes]
rs952507	1.00[JPT][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180477400-180488200	Weak transcription	Pancreas	Pancrea
2	chr2:180478800-180488200	Weak transcription	Lung	lung
3	chr2:180479000-180487400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr2:180483400-180486400	Weak transcription	Fetal Heart	heart
5	chr2:180484000-180487200	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr2:180486000-180494600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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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