Variant report

Variant	rs11129600
Chromosome Location	chr3:34613720-34613721
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]
rs34234856	0.93[ASN][1000 genomes]
rs60041320	0.81[ASN][1000 genomes]
rs6773245	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6788571	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6790851	0.81[ASN][1000 genomes]
rs73060667	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73060691	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9311059	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9881586	0.91[ASN][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:34611400-34614800	Weak transcription	Fetal Heart	heart
2	chr3:34613400-34613800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:34613400-34615000	Weak transcription	H1 BMP4 Derived Mesendoderm 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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