Variant report

Variant	rs6809132
Chromosome Location	chr3:34961680-34961681
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs1522977	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7652900	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:34960400-34963000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr3:34960600-34963200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr3:34961000-34962200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr3:34961400-34961800	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr3:34961600-34962800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr3:34961600-34963000	Enhancers	Breast Myoepithelial Primary Cells	Breast

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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