Variant report

Variant	rs9403841
Chromosome Location	chr6:147290206-147290207
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs17076483	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9373517	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9377039	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9390446	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9403839	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147288200-147291000	Enhancers	Fetal Heart	heart
2	chr6:147289200-147291200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr6:147289200-147294200	Weak transcription	Hela-S3	cervix
4	chr6:147289800-147291200	Weak transcription	Osteobl	bone
5	chr6:147290000-147291200	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr6:147290200-147290600	Weak transcription	Adipose Derived Mesenchymal Stem Cell 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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