Variant report

Variant	rs9377053
Chromosome Location	chr6:147826198-147826199
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs12234160	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9377052	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9377055	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9390470	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9390471	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9390472	0.91[AFR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9399604	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9403858	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9485188	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9485189	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9485190	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9485191	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9485192	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9485194	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9497792	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147821000-147827800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr6:147825200-147827800	Weak transcription	Brain Germinal Matrix	brain

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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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