Variant report

Variant	rs10003328
Chromosome Location	chr4:30687052-30687053
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10005883	0.93[JPT][hapmap];0.81[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs10939311	0.97[ASN][1000 genomes]
rs13105058	0.89[CHD][hapmap];0.84[GIH][hapmap];0.93[JPT][hapmap];0.89[MEX][hapmap];0.88[ASN][1000 genomes]
rs1486767	0.88[CHB][hapmap];0.93[CHD][hapmap];0.84[GIH][hapmap];0.93[JPT][hapmap];0.90[MEX][hapmap];0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6448718	0.84[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs7668393	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9918044	0.86[ASN][1000 genomes]

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10003328	ZFP1	trans	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:30687000-30689400	Enhancers	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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