Variant report

Variant	rs9311059
Chromosome Location	chr3:34610315-34610316
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11129600	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34234856	0.94[ASN][1000 genomes]
rs60041320	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6773245	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6788571	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6792099	0.84[YRI][hapmap]
rs73060667	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73060691	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9881586	0.92[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:34608000-34611400	Enhancers	Fetal Heart	heart
2	chr3:34609200-34610600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:34609400-34612600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr3:34610000-34611000	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr3:34610000-34611400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr3:34610200-34611200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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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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