Variant report

Variant	rs1393394
Chromosome Location	chr1:217318183-217318184
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11579368	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11579388	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11584604	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11585011	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1502351	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73107023	1.00[EUR][1000 genomes]
rs7540820	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:217314200-217318200	Weak transcription	Aorta	Aorta
2	chr1:217317200-217318400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr1:217317800-217318400	Enhancers	Breast Myoepithelial Primary Cells	Breast

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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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