Variant report

Variant	rs463166
Chromosome Location	chr21:40007574-40007575
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1015748	1.00[EUR][1000 genomes]
rs460049	0.83[ASN][1000 genomes]
rs460439	0.85[ASN][1000 genomes]
rs460667	0.85[CHB][hapmap];0.80[ASN][1000 genomes]
rs462006	0.89[JPT][hapmap];0.85[ASN][1000 genomes]
rs463763	0.86[ASN][1000 genomes]
rs463780	1.00[CHB][hapmap];0.96[ASN][1000 genomes]
rs466939	0.95[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];0.84[JPT][hapmap];0.91[ASN][1000 genomes]
rs57208731	1.00[EUR][1000 genomes]
rs57446125	1.00[EUR][1000 genomes]
rs8132169	1.00[EUR][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:40003000-40008600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr21:40003800-40007600	Weak transcription	Aorta	Aorta
3	chr21:40003800-40014400	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr21:40004200-40008800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr21:40006800-40008400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast

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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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