Variant report

Variant	rs7746264
Chromosome Location	chr6:82346792-82346793
allele	C/T
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]
rs12195880	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12198522	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12198609	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12204212	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12208456	0.90[EUR][1000 genomes]
rs12213661	1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4706144	0.85[ASN][1000 genomes]
rs58555568	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6906639	0.85[ASN][1000 genomes]
rs73750612	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73750616	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:82318000-82356600	Weak transcription	Aorta	Aorta
2	chr6:82344800-82348600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:82345200-82348400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:82346200-82347200	Enhancers	Hela-S3	cervix
5	chr6:82346600-82346800	Enhancers	Placenta Amnion	Placenta Amnion
6	chr6:82346600-82347000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr6:82346600-82347400	Enhancers	Muscle Satellite Cultured Cells	--
8	chr6:82346600-82347600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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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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